Variant ID: 16-57006590-C-T

NM_000078.2(CETP):c.750+595C>T

This variant was identified in 68 publications




Publications:


Iterative hard thresholding in genome-wide association studies: Generalized linear models, prior weights, and double sparsity.

Gigascience
BB Chu, KL Keys, CA German, H Zhou, JJ Zhou, EM Sobel, JS Sinsheimer, K Lange
Publication Date: 2020-06-01

Variant appearance in text: rs7499892
PubMed Link: 32491161
Variant Present in the following documents:
  • Main text
View BVdb publication page



The Effect of Haplotypes in the CETP and LIPC Genes on the Triglycerides to HDL-C Ratio and Its Components in the Roma and Hungarian General Populations.

Genes
P Piko, S Fiatal, NA Werissa, BB Bekele, G Racz, Z Kosa, J Sandor, R Adany
Publication Date: 2020-01-03

Variant appearance in text: rs7499892
PubMed Link: 31947886
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association study of metabolic syndrome in Korean populations.

Plos One
SW Oh, JE Lee, E Shin, H Kwon, EK Choe, SY Choi, H Rhee, SH Choi
Publication Date: 2020

Variant appearance in text: rs7499892
PubMed Link: 31910446
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic architecture of human plasma lipidome and its link to cardiovascular disease.

Nature Communications
R Tabassum, JT Rämö, P Ripatti, JT Koskela, M Kurki, J Karjalainen, P Palta, S Hassan, J Nunez-Fontarnau, TTJ Kiiskinen, S Söderlund, N Matikainen, MJ Gerl, MA Surma, C Klose, NO Stitziel, H Laivuori, AS Havulinna, SK Service, V Salomaa, M Pirinen, , M Jauhiainen, MJ Daly, NB Freimer, A Palotie, MR Taskinen, K Simons, S Ripatti
Publication Date: 2019-09-24

Variant appearance in text: rs7499892
PubMed Link: 31551469
Variant Present in the following documents:
  • 41467_2019_11954_MOESM13_ESM.xlsx
  • 41467_2019_11954_MOESM14_ESM.xlsx
View BVdb publication page



The transferability of lipid loci across African, Asian and European cohorts.

Nature Communications
K Kuchenbaecker, N Telkar, T Reiker, RG Walters, K Lin, A Eriksson, D Gurdasani, A Gilly, L Southam, E Tsafantakis, M Karaleftheri, J Seeley, A Kamali, G Asiki, IY Millwood, M Holmes, H Du, Y Guo, M Kumari, G Dedoussis, L Li, Z Chen, MS Sandhu, E Zeggini,
Publication Date: 2019-09-24

Variant appearance in text: rs7499892
PubMed Link: 31551420
Variant Present in the following documents:
  • 41467_2019_12026_MOESM2_ESM.pdf
View BVdb publication page



Subset-Based Analysis Using Gene-Environment Interactions for Discovery of Genetic Associations across Multiple Studies or Phenotypes.

Human Heredity
Y Yu, L Xia, S Lee, X Zhou, HM Stringham, M Boehnke, B Mukherjee
Publication Date: 2018

Variant appearance in text: rs7499892
PubMed Link: 31132756
Variant Present in the following documents:
  • Main text
View BVdb publication page



A PheWAS study of a large observational epidemiological cohort of African Americans from the REGARDS study.

Bmc Medical Genomics
X Zhao, X Geng, V Srinivasasainagendra, N Chaudhary, S Judd, V Wadley, OM Gutiérrez, H Wang, EM Lange, LA Lange, D Woo, FW Unverzagt, M Safford, M Cushman, N Limdi, R Quarells, DK Arnett, MR Irvin, D Zhi
Publication Date: 2019-01-31

Variant appearance in text: rs7499892
PubMed Link: 30704471
Variant Present in the following documents:
  • Main text
View BVdb publication page



Gene-Based Elevated Triglycerides and Type 2 Diabetes Mellitus Risk in the Women's Genome Health Study.

Arteriosclerosis, Thrombosis, And Vascular Biology
S Ahmad, S Mora, PM Ridker, FB Hu, DI Chasman
Publication Date: 2019-01

Variant appearance in text: rs7499892
PubMed Link: 30565958
Variant Present in the following documents:
  • NIHMS1512616-supplement-Supplemental_Material.pdf
View BVdb publication page



Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease.

Alzheimer'S & Dementia (Amsterdam, Netherlands)
GM Peloso, SJ van der Lee, , AL Destefano, S Seshardi
Publication Date: 2018

Variant appearance in text: rs7499892
PubMed Link: 30422133
Variant Present in the following documents:
  • Main text
View BVdb publication page



The role of genetic variation of human metabolism for BMI, mental traits and mental disorders.

Molecular Metabolism
J Hebebrand, T Peters, D Schijven, M Hebebrand, C Grasemann, TW Winkler, IM Heid, J Antel, M Föcker, L Tegeler, L Brauner, RAH Adan, JJ Luykx, CU Correll, IR König, A Hinney, L Libuda
Publication Date: 2018-06

Variant appearance in text: rs7499892
PubMed Link: 29673576
Variant Present in the following documents:
  • mmc1.xlsx
View BVdb publication page



Genetic variations of cholesteryl ester transfer protein and diet interactions in relation to lipid profiles and coronary heart disease: a systematic review.

Nutrition & Metabolism
P Mirmiran, Z Esfandiar, F Hosseini-Esfahani, G Koochakpoor, MS Daneshpour, B Sedaghati-Khayat, F Azizi
Publication Date: 2017

Variant appearance in text: rs7499892
PubMed Link: 29234452
Variant Present in the following documents:
  • 12986_2017_231_MOESM1_ESM.docx
View BVdb publication page



Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.

Plos Genetics
JP Davis, JR Huyghe, AE Locke, AU Jackson, X Sim, HM Stringham, TM Teslovich, RP Welch, C Fuchsberger, N Narisu, PS Chines, AJ Kangas, P Soininen, M Ala-Korpela, J Kuusisto, FS Collins, M Laakso, M Boehnke, KL Mohlke
Publication Date: 2017-10

Variant appearance in text: rs7499892
PubMed Link: 29084231
Variant Present in the following documents:
  • pgen.1007079.s010.xlsx
View BVdb publication page



Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease.

Nature Genetics
X Lu, GM Peloso, DJ Liu, Y Wu, H Zhang, W Zhou, J Li, CS Tang, R Dorajoo, H Li, J Long, X Guo, M Xu, CN Spracklen, Y Chen, X Liu, Y Zhang, CC Khor, J Liu, L Sun, L Wang, YT Gao, Y Hu, K Yu, Y Wang, CYY Cheung, F Wang, J Huang, Q Fan, Q Cai, S Chen, J Shi, X Yang, W Zhao, WH Sheu, SS Cherny, M He, AB Feranil, LS Adair, P Gordon-Larsen, S Du, R Varma, YI Chen, XO Shu, KSL Lam, TY Wong, SK Ganesh, Z Mo, K Hveem, LG Fritsche, JB Nielsen, HF Tse, Y Huo, CY Cheng, YE Chen, W Zheng, ES Tai, W Gao, X Lin, W Huang, G Abecasis, , S Kathiresan, KL Mohlke, T Wu, PC Sham, D Gu, CJ Willer
Publication Date: 2017-12

Variant appearance in text: rs7499892
PubMed Link: 29083407
Variant Present in the following documents:
  • NIHMS909133-supplement-1.docx
  • NIHMS909133-supplement-2.xlsx
View BVdb publication page



PLATO software provides analytic framework for investigating complexity beyond genome-wide association studies.

Nature Communications
MA Hall, J Wallace, A Lucas, D Kim, AO Basile, SS Verma, CA McCarty, MH Brilliant, PL Peissig, TE Kitchner, A Verma, SA Pendergrass, SM Dudek, JH Moore, MD Ritchie
Publication Date: 2017-10-27

Variant appearance in text: rs7499892
PubMed Link: 29079728
Variant Present in the following documents:
  • Main text
View BVdb publication page



Iterative hard thresholding for model selection in genome-wide association studies.

Genetic Epidemiology
KL Keys, GK Chen, K Lange
Publication Date: 2017-12

Variant appearance in text: rs7499892
PubMed Link: 28875524
Variant Present in the following documents:
  • Main text
  • NIHMS898446-supplement-Supp_TableS1-2.docx
View BVdb publication page



A Scalable Bayesian Method for Integrating Functional Information in Genome-wide Association Studies.

American Journal Of Human Genetics
J Yang, LG Fritsche, X Zhou, G Abecasis,
Publication Date: 2017-09-07

Variant appearance in text: rs7499892
PubMed Link: 28844487
Variant Present in the following documents:
  • mmc1.pdf
  • mmc2.pdf
View BVdb publication page



Data to genetic risk assessment on high-density cholesterol level associated polymorphisms in Hungarian general and Roma populations.

Data In Brief
P Pikó, S Fiatal, Z Kósa, J Sándor, R Ádány
Publication Date: 2017-10

Variant appearance in text: rs7499892
PubMed Link: 28795114
Variant Present in the following documents:
  • Main text
View BVdb publication page



Fine mapping the CETP region reveals a common intronic insertion associated to HDL-C.

Npj Aging And Mechanisms Of Disease
EM van Leeuwen, JE Huffman, JC Bis, A Isaacs, M Mulder, A Sabo, AV Smith, S Demissie, A Manichaikul, JA Brody, MF Feitosa, Q Duan, KE Schraut, P Navarro, JV van Vliet-Ostaptchouk, G Zhu, H Mbarek, S Trompet, N Verweij, LP Lyytikäinen, J Deelen, IM Nolte, SW van der Laan, G Davies, AJ Vermeij-Verdoold, AA van Oosterhout, JM Vergeer-Drop, DE Arking, H Trochet, , C Medina-Gomez, F Rivadeneira, AG Uitterlinden, A Dehghan, OH Franco, EJ Sijbrands, A Hofman, CC White, JC Mychaleckyj, GM Peloso, MA Swertz, , G Willemsen, EJ de Geus, Y Milaneschi, BW Penninx, I Ford, BM Buckley, AJ de Craen, JM Starr, IJ Deary, G Pasterkamp, AJ Oldehinkel, H Snieder, PE Slagboom, K Nikus, M Kähönen, T Lehtimäki, JS Viikari, OT Raitakari, P van der Harst, JW Jukema, JJ Hottenga, DI Boomsma, JB Whitfield, G Montgomery, NG Martin, , O Polasek, V Vitart, C Hayward, I Kolcic, AF Wright, I Rudan, PK Joshi, JF Wilson, LA Lange, JG Wilson, V Gudnason, TB Harris, AC Morrison, IB Borecki, SS Rich, S Padmanabhan, BM Psaty, JI Rotter, BH Smith, E Boerwinkle, LA Cupples, C van Duijn
Publication Date: 2015

Variant appearance in text: rs7499892
PubMed Link: 28721259
Variant Present in the following documents:
  • Main text
  • npjamd201511-s1.doc
View BVdb publication page



Replication and fine-mapping of genetic predictors of lipid traits in African-Americans.

Journal Of Human Genetics
Q Feng, WQ Wei, RT Levinson, JD Mosley, CM Stein
Publication Date: 2017-10

Variant appearance in text: rs7499892
PubMed Link: 28539666
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of eight genetic variants as novel determinants of dyslipidemia in Japanese by exome-wide association studies.

Oncotarget
Y Yamada, J Sakuma, I Takeuchi, Y Yasukochi, K Kato, M Oguri, T Fujimaki, H Horibe, M Muramatsu, M Sawabe, Y Fujiwara, Y Taniguchi, S Obuchi, H Kawai, S Shinkai, S Mori, T Arai, M Tanaka
Publication Date: 2017-06-13

Variant appearance in text: rs7499892
PubMed Link: 28473662
Variant Present in the following documents:
  • oncotarget-08-38950-s002.docx
  • oncotarget-08-38950-s013.docx
  • oncotarget-08-38950-s016.docx
  • oncotarget-08-38950-s019.docx
View BVdb publication page



Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci.

Human Molecular Genetics
N Zubair, M Graff, J Luis Ambite, WS Bush, G Kichaev, Y Lu, A Manichaikul, WH Sheu, D Absher, TL Assimes, SJ Bielinski, EP Bottinger, P Buzkova, LM Chuang, RH Chung, B Cochran, L Dumitrescu, O Gottesman, JW Haessler, C Haiman, G Heiss, CA Hsiung, YJ Hung, CM Hwu, JJ Juang, L Le Marchand, IT Lee, WJ Lee, LA Lin, D Lin, SY Lin, RH Mackey, LW Martin, B Pasaniuc, U Peters, I Predazzi, T Quertermous, AP Reiner, J Robinson, JI Rotter, KK Ryckman, PJ Schreiner, E Stahl, R Tao, MY Tsai, LL Waite, TD Wang, S Buyske, YD Ida Chen, I Cheng, DC Crawford, RJF Loos, SS Rich, M Fornage, KE North, C Kooperberg, CL Carty
Publication Date: 2016-12-15

Variant appearance in text: rs7499892
PubMed Link: 28426890
Variant Present in the following documents:
  • ddw358_supp.docx
View BVdb publication page



Genetic associations with lipoprotein subfraction measures differ by ethnicity in the multi-ethnic study of atherosclerosis (MESA).

Human Genetics
Z Wang, A Manichukal, DC Goff, S Mora, JM Ordovas, NM Pajewski, WS Post, JI Rotter, MM Sale, SA Santorico, D Siscovick, MY Tsai, DK Arnett, S Rich, AC Frazier-Wood
Publication Date: 2017-06

Variant appearance in text: rs7499892
PubMed Link: 28352986
Variant Present in the following documents:
  • 439_2017_1782_MOESM1_ESM.docx
View BVdb publication page



Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.

Genome Medicine
R Nagy, TS Boutin, J Marten, JE Huffman, SM Kerr, A Campbell, L Evenden, J Gibson, C Amador, DM Howard, P Navarro, A Morris, IJ Deary, LJ Hocking, S Padmanabhan, BH Smith, P Joshi, JF Wilson, ND Hastie, AF Wright, AM McIntosh, DJ Porteous, CS Haley, V Vitart, C Hayward
Publication Date: 2017-03-07

Variant appearance in text: rs7499892
PubMed Link: 28270201
Variant Present in the following documents:
  • 13073_2017_414_MOESM9_ESM.xlsx
View BVdb publication page



Association and interaction of APOA5, BUD13, CETP, LIPA and health-related behavior with metabolic syndrome in a Taiwanese population.

Scientific Reports
E Lin, PH Kuo, YL Liu, AC Yang, CF Kao, SJ Tsai
Publication Date: 2016-11-09

Variant appearance in text: rs7499892
PubMed Link: 27827461
Variant Present in the following documents:
  • srep36830-s1.pdf
View BVdb publication page



c.*84G>A Mutation in CETP Is Associated with Coronary Artery Disease in South Indians.

Plos One
M Ganesan, S Nizamuddin, SK Katkam, K Kumaraswami, UK Hosad, LL Lobo, VK Kutala, K Thangaraj
Publication Date: 2016

Variant appearance in text: rs7499892
PubMed Link: 27768712
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variants in CETP increase risk of intracerebral hemorrhage.

Annals Of Neurology
CD Anderson, GJ Falcone, CL Phuah, F Radmanesh, HB Brouwers, TW Battey, A Biffi, GM Peloso, DJ Liu, AM Ayres, JN Goldstein, A Viswanathan, SM Greenberg, M Selim, JF Meschia, DL Brown, BB Worrall, SL Silliman, DL Tirschwell, ML Flaherty, P Kraft, JM Jagiella, H Schmidt, BM Hansen, J Jimenez-Conde, E Giralt-Steinhauer, R Elosua, E Cuadrado-Godia, C Soriano, KM van Nieuwenhuizen, CJ Klijn, K Rannikmae, N Samarasekera, R Al-Shahi Salman, CL Sudlow, IJ Deary, A Morotti, A Pezzini, J Pera, A Urbanik, A Pichler, C Enzinger, B Norrving, J Montaner, I Fernandez-Cadenas, P Delgado, J Roquer, A Lindgren, A Slowik, R Schmidt, CS Kidwell, SJ Kittner, SP Waddy, CD Langefeld, G Abecasis, CJ Willer, S Kathiresan, D Woo, J Rosand,
Publication Date: 2016-11

Variant appearance in text: rs7499892
PubMed Link: 27717122
Variant Present in the following documents:
  • Main text
View BVdb publication page



Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.

Nature Genetics
V Iotchkova, J Huang, JA Morris, D Jain, C Barbieri, K Walter, JL Min, L Chen, W Astle, M Cocca, P Deelen, H Elding, AE Farmaki, CS Franklin, M Franberg, TR Gaunt, A Hofman, T Jiang, ME Kleber, G Lachance, J Luan, G Malerba, A Matchan, D Mead, Y Memari, I Ntalla, K Panoutsopoulou, R Pazoki, JRB Perry, F Rivadeneira, M Sabater-Lleal, B Sennblad, SY Shin, L Southam, M Traglia, F van Dijk, EM van Leeuwen, G Zaza, W Zhang, , N Amin, A Butterworth, JC Chambers, G Dedoussis, A Dehghan, OH Franco, L Franke, M Frontini, G Gambaro, P Gasparini, A Hamsten, A Issacs, JS Kooner, C Kooperberg, C Langenberg, W Marz, RA Scott, MA Swertz, D Toniolo, AG Uitterlinden, CM van Duijn, H Watkins, E Zeggini, MT Maurano, NJ Timpson, AP Reiner, PL Auer, N Soranzo
Publication Date: 2016-11

Variant appearance in text: rs7499892
PubMed Link: 27668658
Variant Present in the following documents:
  • NIHMS71079-supplement-Supplementary_Data.pdf
View BVdb publication page



Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs.

Scientific Reports
JE Below, EJ Parra, ER Gamazon, J Torres, S Krithika, S Candille, Y Lu, A Manichakul, J Peralta-Romero, Q Duan, Y Li, AP Morris, O Gottesman, E Bottinger, XQ Wang, KD Taylor, YD Ida Chen, JI Rotter, SS Rich, RJ Loos, H Tang, NJ Cox, M Cruz, CL Hanis, A Valladares-Salgado
Publication Date: 2016-01-19

Variant appearance in text: rs7499892
PubMed Link: 26780889
Variant Present in the following documents:
  • Main text
  • srep19429-s1.pdf
  • srep19429-s3.xls
  • srep19429-s5.xls
View BVdb publication page



INTEGRATING CLINICAL LABORATORY MEASURES AND ICD-9 CODE DIAGNOSES IN PHENOME-WIDE ASSOCIATION STUDIES.

Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing
A Verma, JB Leader, SS Verma, A Frase, J Wallace, S Dudek, DR Lavage, CV Van Hout, FE Dewey, J Penn, A Lopez, JD Overton, DJ Carey, DH Ledbetter, HL Kirchner, MD Ritchie, SA Pendergrass
Publication Date: 2016

Variant appearance in text: rs7499892
PubMed Link: 26776183
Variant Present in the following documents:
  • NIHMS742521-supplement-2.pdf
View BVdb publication page



Regional heritability mapping method helps explain missing heritability of blood lipid traits in isolated populations.

Heredity
M Shirali, R Pong-Wong, P Navarro, S Knott, C Hayward, V Vitart, I Rudan, H Campbell, ND Hastie, AF Wright, CS Haley
Publication Date: 2016-03

Variant appearance in text: rs7499892
PubMed Link: 26696135
Variant Present in the following documents:
  • Main text
  • hdy2015107x1.docx
View BVdb publication page



Resequencing of the CETP gene in American whites and African blacks: Association of rare and common variants with HDL-cholesterol levels.

Metabolism: Clinical And Experimental
D Pirim, X Wang, V Niemsiri, ZH Radwan, CH Bunker, JE Hokanson, RF Hamman, MM Barmada, FY Demirci, MI Kamboh
Publication Date: 2016-01

Variant appearance in text: rs7499892
PubMed Link: 26683795
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genomic prediction of complex human traits: relatedness, trait architecture and predictive meta-models.

Human Molecular Genetics
A Spiliopoulou, R Nagy, ML Bermingham, JE Huffman, C Hayward, V Vitart, I Rudan, H Campbell, AF Wright, JF Wilson, R Pong-Wong, F Agakov, P Navarro, CS Haley
Publication Date: 2015-07-15

Variant appearance in text: rs7499892
PubMed Link: 25918167
Variant Present in the following documents:
  • Main text
View BVdb publication page



A multivariate genome-wide association analysis of 10 LDL subfractions, and their response to statin treatment, in 1868 Caucasians.

Plos One
H Shim, DI Chasman, JD Smith, S Mora, PM Ridker, DA Nickerson, RM Krauss, M Stephens
Publication Date: 2015

Variant appearance in text: rs7499892
PubMed Link: 25898129
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetics of kidney disease and related cardiometabolic phenotypes in Zuni Indians: the Zuni Kidney Project.

Frontiers In Genetics
SL Laston, VS Voruganti, K Haack, VO Shah, A Bobelu, J Bobelu, D Ghahate, AM Harford, SS Paine, F Tentori, SA Cole, JW MacCluer, AG Comuzzie, PG Zager
Publication Date: 2015

Variant appearance in text: rs7499892
PubMed Link: 25688259
Variant Present in the following documents:
  • Main text
View BVdb publication page



New loci and coding variants confer risk for age-related macular degeneration in East Asians.

Nature Communications
CY Cheng, K Yamashiro, LJ Chen, J Ahn, L Huang, L Huang, CM Cheung, M Miyake, PD Cackett, IY Yeo, A Laude, R Mathur, J Pang, KS Sim, AH Koh, P Chen, SY Lee, D Wong, CM Chan, BK Loh, Y Sun, S Davila, I Nakata, H Nakanishi, Y Akagi-Kurashige, N Gotoh, A Tsujikawa, F Matsuda, K Mori, S Yoneya, Y Sakurada, H Iijima, T Iida, S Honda, TY Lai, PO Tam, H Chen, S Tang, X Ding, F Wen, F Lu, X Zhang, Y Shi, P Zhao, B Zhao, J Sang, B Gong, R Dorajoo, JM Yuan, WP Koh, RM van Dam, Y Friedlander, Y Lin, ML Hibberd, JN Foo, N Wang, CH Wong, GS Tan, SJ Park, M Bhargava, L Gopal, T Naing, J Liao, PG Ong, P Mitchell, P Zhou, X Xie, J Liang, J Mei, X Jin, SM Saw, M Ozaki, T Mizoguchi, Y Kurimoto, SJ Woo, H Chung, HG Yu, JY Shin, DH Park, IT Kim, W Chang, M Sagong, SJ Lee, HW Kim, JE Lee, Y Li, J Liu, YY Teo, CK Heng, TH Lim, SK Yang, K Song, EN Vithana, T Aung, JX Bei, YX Zeng, ES Tai, XX Li, Z Yang, KH Park, CP Pang, N Yoshimura, TY Wong, CC Khor
Publication Date: 2015-01-28

Variant appearance in text: rs7499892
PubMed Link: 25629512
Variant Present in the following documents:
  • ncomms7063-s1.pdf
View BVdb publication page



Association between CETP, MLXIPL, and TOMM40 polymorphisms and serum lipid levels in a Latvian population.

Meta Gene
I Radovica, D Fridmanis, I Silamikelis, L Nikitina-Zake, J Klovins
Publication Date: 2014-12

Variant appearance in text: rs7499892
PubMed Link: 25606439
Variant Present in the following documents:
  • mmc2.docx
View BVdb publication page



MGAS: a powerful tool for multivariate gene-based genome-wide association analysis.

Bioinformatics (Oxford, England)
S Van der Sluis, CV Dolan, J Li, Y Song, P Sham, D Posthuma, MX Li
Publication Date: 2015-04-01

Variant appearance in text: rs7499892
PubMed Link: 25431328
Variant Present in the following documents:
  • Main text
View BVdb publication page



Analysis of metabolic syndrome components in >15 000 african americans identifies pleiotropic variants: results from the population architecture using genomics and epidemiology study.

Circulation. Cardiovascular Genetics
CL Carty, S Bhattacharjee, J Haessler, I Cheng, LA Hindorff, V Aroda, CS Carlson, CN Hsu, L Wilkens, S Liu, E Selvin, R Jackson, KE North, U Peters, JS Pankow, N Chatterjee, C Kooperberg
Publication Date: 2014-08

Variant appearance in text: rs7499892
PubMed Link: 25023634
Variant Present in the following documents:
  • Main text
  • NIHMS614064-supplement-000386_-_PAP.pdf
View BVdb publication page



Genome-wide family-based linkage analysis of exome chip variants and cardiometabolic risk.

Genetic Epidemiology
JN Hellwege, ND Palmer, LM Raffield, MC Ng, GA Hawkins, J Long, C Lorenzo, JM Norris, YD Ida Chen, EK Speliotes, JI Rotter, CD Langefeld, LE Wagenknecht, DW Bowden
Publication Date: 2014-05

Variant appearance in text: rs7499892
PubMed Link: 24719370
Variant Present in the following documents:
  • Main text
  • NIHMS649741-supplement-supplemental_tables.docx
View BVdb publication page



CETP gene polymorphisms and risk of coronary atherosclerosis in a Chinese population.

Lipids In Health And Disease
J Wang, LJ Wang, Y Zhong, P Gu, JQ Shao, SS Jiang, JB Gong
Publication Date: 2013-11-27

Variant appearance in text: rs7499892
PubMed Link: 24283500
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic association with lipids in Filipinos: waist circumference modifies an APOA5 effect on triglyceride levels.

Journal Of Lipid Research
Y Wu, AF Marvelle, J Li, DC Croteau-Chonka, AB Feranil, CW Kuzawa, Y Li, LS Adair, KL Mohlke
Publication Date: 2013-11

Variant appearance in text: rs7499892
PubMed Link: 24023260
Variant Present in the following documents:
  • Main text
View BVdb publication page



Properties of local interactions and their potential value in complementing genome-wide association studies.

Plos One
W Wei, A Gyenesei, CA Semple, CS Haley
Publication Date: 2013

Variant appearance in text: rs7499892
PubMed Link: 23940718
Variant Present in the following documents:
  • Main text
  • pone.0071203.s003.xlsx
View BVdb publication page



Single nucleotide polymorphisms in CETP, SLC46A1, SLC19A1, CD36, BCMO1, APOA5, and ABCA1 are significant predictors of plasma HDL in healthy adults.

Lipids In Health And Disease
AJ Clifford, G Rincon, JE Owens, JF Medrano, AJ Moshfegh, DJ Baer, JA Novotny
Publication Date: 2013-05-08

Variant appearance in text: rs7499892
PubMed Link: 23656756
Variant Present in the following documents:
  • Main text
View BVdb publication page



Investigation of gene-by-sex interactions for lipid traits in diverse populations from the population architecture using genomics and epidemiology study.

Bmc Genetics
KC Taylor, CL Carty, L Dumitrescu, P Bůžková, SA Cole, L Hindorff, FR Schumacher, LR Wilkens, RV Shohet, PM Quibrera, KC Johnson, BE Henderson, J Haessler, N Franceschini, CB Eaton, DJ Duggan, B Cochran, I Cheng, CS Carlson, K Brown-Gentry, G Anderson, JL Ambite, C Haiman, L Le Marchand, C Kooperberg, DC Crawford, S Buyske, KE North, M Fornage,
Publication Date: 2013-05-01

Variant appearance in text: rs7499892
PubMed Link: 23634756
Variant Present in the following documents:
  • Main text
View BVdb publication page



Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained.

Plos Genetics
Y Wu, LL Waite, AU Jackson, WH Sheu, S Buyske, D Absher, DK Arnett, E Boerwinkle, LL Bonnycastle, CL Carty, I Cheng, B Cochran, DC Croteau-Chonka, L Dumitrescu, CB Eaton, N Franceschini, X Guo, BE Henderson, LA Hindorff, E Kim, L Kinnunen, P Komulainen, WJ Lee, L Le Marchand, Y Lin, J Lindström, O Lingaas-Holmen, SL Mitchell, N Narisu, JG Robinson, F Schumacher, A Stančáková, J Sundvall, YJ Sung, AJ Swift, WC Wang, L Wilkens, T Wilsgaard, AM Young, LS Adair, CM Ballantyne, P Bůžková, A Chakravarti, FS Collins, D Duggan, AB Feranil, LT Ho, YJ Hung, SC Hunt, K Hveem, JM Juang, AY Kesäniemi, J Kuusisto, M Laakso, TA Lakka, IT Lee, MF Leppert, TC Matise, L Moilanen, I Njølstad, U Peters, T Quertermous, R Rauramaa, JI Rotter, J Saramies, J Tuomilehto, M Uusitupa, TD Wang, M Boehnke, CA Haiman, YD Chen, C Kooperberg, TL Assimes, DC Crawford, CA Hsiung, KE North, KL Mohlke
Publication Date: 2013-03

Variant appearance in text: rs7499892
PubMed Link: 23555291
Variant Present in the following documents:
  • Main text
View BVdb publication page



Seven new loci associated with age-related macular degeneration.

Nature Genetics
LG Fritsche, W Chen, M Schu, BL Yaspan, Y Yu, G Thorleifsson, DJ Zack, S Arakawa, V Cipriani, S Ripke, RP Igo, GH Buitendijk, X Sim, DE Weeks, RH Guymer, JE Merriam, PJ Francis, G Hannum, A Agarwal, AM Armbrecht, I Audo, T Aung, GR Barile, M Benchaboune, AC Bird, PN Bishop, KE Branham, M Brooks, AJ Brucker, WH Cade, MS Cain, PA Campochiaro, CC Chan, CY Cheng, EY Chew, KA Chin, I Chowers, DG Clayton, R Cojocaru, YP Conley, BK Cornes, MJ Daly, B Dhillon, AO Edwards, E Evangelou, J Fagerness, HA Ferreyra, JS Friedman, A Geirsdottir, RJ George, C Gieger, N Gupta, SA Hagstrom, SP Harding, C Haritoglou, JR Heckenlively, FG Holz, G Hughes, JP Ioannidis, T Ishibashi, P Joseph, G Jun, Y Kamatani, N Katsanis, C N Keilhauer, JC Khan, IK Kim, Y Kiyohara, BE Klein, R Klein, JL Kovach, I Kozak, CJ Lee, KE Lee, P Lichtner, AJ Lotery, T Meitinger, P Mitchell, S Mohand-Saïd, AT Moore, DJ Morgan, MA Morrison, CE Myers, AC Naj, Y Nakamura, Y Okada, A Orlin, MC Ortube, MI Othman, C Pappas, KH Park, GJ Pauer, NS Peachey, O Poch, RR Priya, R Reynolds, AJ Richardson, R Ripp, G Rudolph, E Ryu, JA Sahel, DA Schaumberg, HP Scholl, SG Schwartz, WK Scott, H Shahid, H Sigurdsson, G Silvestri, TA Sivakumaran, RT Smith, L Sobrin, EH Souied, DE Stambolian, H Stefansson, GM Sturgill-Short, A Takahashi, N Tosakulwong, BJ Truitt, EE Tsironi, AG Uitterlinden, CM van Duijn, L Vijaya, JR Vingerling, EN Vithana, AR Webster, HE Wichmann, TW Winkler, TY Wong, AF Wright, D Zelenika, M Zhang, L Zhao, K Zhang, ML Klein, GS Hageman, GM Lathrop, K Stefansson, R Allikmets, PN Baird, MB Gorin, JJ Wang, CC Klaver, JM Seddon, MA Pericak-Vance, SK Iyengar, JR Yates, A Swaroop, BH Weber, M Kubo, MM Deangelis, T Léveillard, U Thorsteinsdottir, JL Haines, LA Farrer, IM Heid, GR Abecasis,
Publication Date: 2013-04

Variant appearance in text: rs7499892
PubMed Link: 23455636
Variant Present in the following documents:
  • NIHMS474886-supplement-1.pdf
View BVdb publication page



Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations.

Plos One
CC Elbers, Y Guo, V Tragante, EP van Iperen, MB Lanktree, BA Castillo, F Chen, LR Yanek, MK Wojczynski, YR Li, B Ferwerda, CM Ballantyne, SG Buxbaum, YD Chen, WM Chen, LA Cupples, M Cushman, Y Duan, D Duggan, MK Evans, JK Fernandes, M Fornage, M Garcia, WT Garvey, N Glazer, F Gomez, TB Harris, I Halder, VJ Howard, MF Keller, MI Kamboh, C Kooperberg, SB Kritchevsky, A LaCroix, K Liu, Y Liu, K Musunuru, AB Newman, NC Onland-Moret, J Ordovas, I Peter, W Post, S Redline, SE Reis, R Saxena, PJ Schreiner, KA Volcik, X Wang, S Yusuf, AB Zonderland, SS Anand, DM Becker, B Psaty, DJ Rader, AP Reiner, SS Rich, JI Rotter, MM Sale, MY Tsai, IB Borecki, RA Hegele, S Kathiresan, MA Nalls, HA Taylor, H Hakonarson, S Sivapalaratnam, FW Asselbergs, F Drenos, JG Wilson, BJ Keating
Publication Date: 2012

Variant appearance in text: rs7499892
PubMed Link: 23236364
Variant Present in the following documents:
  • Main text
  • pone.0050198.s007.xlsx
View BVdb publication page



Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.

American Journal Of Human Genetics
FW Asselbergs, Y Guo, EP van Iperen, S Sivapalaratnam, V Tragante, MB Lanktree, LA Lange, B Almoguera, YE Appelman, J Barnard, J Baumert, AL Beitelshees, TR Bhangale, YD Chen, TR Gaunt, Y Gong, JC Hopewell, T Johnson, ME Kleber, TY Langaee, M Li, YR Li, K Liu, CW McDonough, MF Meijs, RP Middelberg, K Musunuru, CP Nelson, JR O'Connell, S Padmanabhan, JS Pankow, N Pankratz, S Rafelt, R Rajagopalan, SP Romaine, NJ Schork, J Shaffer, H Shen, EN Smith, SE Tischfield, PJ van der Most, JV van Vliet-Ostaptchouk, N Verweij, KA Volcik, L Zhang, KR Bailey, KM Bailey, F Bauer, JM Boer, PS Braund, A Burt, PR Burton, SG Buxbaum, W Chen, RM Cooper-Dehoff, LA Cupples, JS deJong, C Delles, D Duggan, M Fornage, CE Furlong, N Glazer, JG Gums, C Hastie, MV Holmes, T Illig, SA Kirkland, M Kivimaki, R Klein, BE Klein, C Kooperberg, K Kottke-Marchant, M Kumari, AZ LaCroix, L Mallela, G Murugesan, J Ordovas, WH Ouwehand, WS Post, R Saxena, H Scharnagl, PJ Schreiner, T Shah, DC Shields, D Shimbo, SR Srinivasan, RP Stolk, DI Swerdlow, HA Taylor, EJ Topol, E Toskala, JL van Pelt, J van Setten, S Yusuf, JC Whittaker, AH Zwinderman, , SS Anand, AJ Balmforth, GS Berenson, CR Bezzina, BO Boehm, E Boerwinkle, JP Casas, MJ Caulfield, R Clarke, JM Connell, KJ Cruickshanks, KW Davidson, IN Day, PI de Bakker, PA Doevendans, AF Dominiczak, AS Hall, CA Hartman, C Hengstenberg, HL Hillege, MH Hofker, SE Humphries, GP Jarvik, JA Johnson, BM Kaess, S Kathiresan, W Koenig, DA Lawlor, W März, O Melander, BD Mitchell, GW Montgomery, PB Munroe, SS Murray, SJ Newhouse, NC Onland-Moret, N Poulter, B Psaty, S Redline, SS Rich, JI Rotter, H Schunkert, P Sever, AR Shuldiner, RL Silverstein, A Stanton, B Thorand, MD Trip, MY Tsai, P van der Harst, E van der Schoot, YT van der Schouw, WM Verschuren, H Watkins, AA Wilde, BH Wolffenbuttel, JB Whitfield, GK Hovingh, CM Ballantyne, C Wijmenga, MP Reilly, NG Martin, JG Wilson, DJ Rader, NJ Samani, AP Reiner, RA Hegele, JJ Kastelein, AD Hingorani, PJ Talmud, H Hakonarson, CC Elbers, BJ Keating, F Drenos
Publication Date: 2012-11-02

Variant appearance in text: rs7499892
PubMed Link: 23063622
Variant Present in the following documents:
  • mmc4.xls
  • mmc5.xls
  • mmc6.xls
  • mmc7.xls
View BVdb publication page



A mixed-model approach for genome-wide association studies of correlated traits in structured populations.

Nature Genetics
A Korte, BJ Vilhjálmsson, V Segura, A Platt, Q Long, M Nordborg
Publication Date: 2012-09

Variant appearance in text: rs7499892
PubMed Link: 22902788
Variant Present in the following documents:
  • NIHMS392993-supplement-1.pdf
View BVdb publication page



An efficient multi-locus mixed-model approach for genome-wide association studies in structured populations.

Nature Genetics
V Segura, BJ Vilhjálmsson, A Platt, A Korte, Ü Seren, Q Long, M Nordborg
Publication Date: 2012-06-17

Variant appearance in text: rs7499892
PubMed Link: 22706313
Variant Present in the following documents:
  • Main text
View BVdb publication page



Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project.

Plos One
K Musunuru, SP Romaine, G Lettre, JG Wilson, KA Volcik, MY Tsai, HA Taylor, PJ Schreiner, JI Rotter, SS Rich, S Redline, BM Psaty, GJ Papanicolaou, JM Ordovas, K Liu, RM Krauss, NL Glazer, SB Gabriel, M Fornage, LA Cupples, SG Buxbaum, E Boerwinkle, CM Ballantyne, S Kathiresan, DJ Rader
Publication Date: 2012

Variant appearance in text: rs7499892
PubMed Link: 22629316
Variant Present in the following documents:
  • Main text
View BVdb publication page



Inherited variation at chromosome 12p13.33, including RAD52, influences the risk of squamous cell lung carcinoma.

Cancer Discovery
J Shi, N Chatterjee, M Rotunno, Y Wang, AC Pesatori, D Consonni, P Li, W Wheeler, P Broderick, M Henrion, T Eisen, Z Wang, W Chen, Q Dong, D Albanes, M Thun, MR Spitz, PA Bertazzi, NE Caporaso, SJ Chanock, CI Amos, RS Houlston, MT Landi
Publication Date: 2012-02

Variant appearance in text: rs7499892
PubMed Link: 22585858
Variant Present in the following documents:
  • NIHMS343818-supplement-1.pdf
View BVdb publication page



Cholesteryl Ester Transfer Protein (CETP) polymorphisms affect mRNA splicing, HDL levels, and sex-dependent cardiovascular risk.

Plos One
AC Papp, JK Pinsonneault, D Wang, LC Newman, Y Gong, JA Johnson, CJ Pepine, M Kumari, AD Hingorani, PJ Talmud, S Shah, SE Humphries, W Sadee
Publication Date: 2012

Variant appearance in text: rs7499892
PubMed Link: 22403620
Variant Present in the following documents:
  • pone.0031930.s009.docx
  • pone.0031930.s010.docx
View BVdb publication page



Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.

Plos Genetics
A Demirkan, CM van Duijn, P Ugocsai, A Isaacs, PP Pramstaller, G Liebisch, JF Wilson, Å Johansson, I Rudan, YS Aulchenko, AV Kirichenko, AC Janssens, RC Jansen, C Gnewuch, FS Domingues, C Pattaro, SH Wild, I Jonasson, O Polasek, IV Zorkoltseva, A Hofman, LC Karssen, M Struchalin, J Floyd, W Igl, Z Biloglav, L Broer, A Pfeufer, I Pichler, S Campbell, G Zaboli, I Kolcic, F Rivadeneira, J Huffman, ND Hastie, A Uitterlinden, L Franke, CS Franklin, V Vitart, , CP Nelson, M Preuss, , JC Bis, CJ O'Donnell, N Franceschini, , JC Witteman, T Axenovich, BA Oostra, T Meitinger, AA Hicks, C Hayward, AF Wright, U Gyllensten, H Campbell, G Schmitz,
Publication Date: 2012

Variant appearance in text: rs7499892
PubMed Link: 22359512
Variant Present in the following documents:
  • pgen.1002490.s009.pdf
View BVdb publication page



Genome-wide association study identifies multiple loci influencing human serum metabolite levels.

Nature Genetics
J Kettunen, T Tukiainen, AP Sarin, A Ortega-Alonso, E Tikkanen, LP Lyytikäinen, AJ Kangas, P Soininen, P Würtz, K Silander, DM Dick, RJ Rose, MJ Savolainen, J Viikari, M Kähönen, T Lehtimäki, KH Pietiläinen, M Inouye, MI McCarthy, A Jula, J Eriksson, OT Raitakari, V Salomaa, J Kaprio, MR Järvelin, L Peltonen, M Perola, NB Freimer, M Ala-Korpela, A Palotie, S Ripatti
Publication Date: 2012-01-29

Variant appearance in text: rs7499892
PubMed Link: 22286219
Variant Present in the following documents:
  • NIHMS444574-supplement-supplementary_table_2.xlsx
View BVdb publication page



A survey of the genetics of stomach, liver, and adipose gene expression from a morbidly obese cohort.

Genome Research
DM Greenawalt, R Dobrin, E Chudin, IJ Hatoum, C Suver, J Beaulaurier, B Zhang, V Castro, J Zhu, SK Sieberts, S Wang, C Molony, SB Heymsfield, DM Kemp, ML Reitman, PY Lum, EE Schadt, LM Kaplan
Publication Date: 2011-07

Variant appearance in text: rs7499892
PubMed Link: 21602305
Variant Present in the following documents:
  • Main text
View BVdb publication page



Knowledge-driven multi-locus analysis reveals gene-gene interactions influencing HDL cholesterol level in two independent EMR-linked biobanks.

Plos One
SD Turner, RL Berg, JG Linneman, PL Peissig, DC Crawford, JC Denny, DM Roden, CA McCarty, MD Ritchie, RA Wilke
Publication Date: 2011-05-11

Variant appearance in text: rs7499892
PubMed Link: 21589926
Variant Present in the following documents:
  • pone.0019586.s004.pdf
View BVdb publication page



Genetic architecture of circulating lipid levels.

European Journal Of Human Genetics : Ejhg
A Demirkan, N Amin, A Isaacs, MR Jarvelin, JB Whitfield, HE Wichmann, KO Kyvik, I Rudan, C Gieger, AA Hicks, Å Johansson, JJ Hottenga, JJ Smith, SH Wild, NL Pedersen, G Willemsen, M Mangino, C Hayward, AG Uitterlinden, A Hofman, J Witteman, GW Montgomery, KH Pietiläinen, T Rantanen, J Kaprio, A Döring, PP Pramstaller, U Gyllensten, EJ de Geus, BW Penninx, JF Wilson, F Rivadeneria, PK Magnusson, DI Boomsma, T Spector, H Campbell, B Hoehne, NG Martin, BA Oostra, M McCarthy, L Peltonen-Palotie, Y Aulchenko, PM Visscher, S Ripatti, AC Janssens, CM van Duijn,
Publication Date: 2011-07

Variant appearance in text: rs7499892
PubMed Link: 21448234
Variant Present in the following documents:
  • Main text
  • ejhg201121x5.doc
View BVdb publication page



Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.

Plos Genetics
G Lettre, CD Palmer, T Young, KG Ejebe, H Allayee, EJ Benjamin, F Bennett, DW Bowden, A Chakravarti, A Dreisbach, DN Farlow, AR Folsom, M Fornage, T Forrester, E Fox, CA Haiman, J Hartiala, TB Harris, SL Hazen, SR Heckbert, BE Henderson, JN Hirschhorn, BJ Keating, SB Kritchevsky, E Larkin, M Li, ME Rudock, CA McKenzie, JB Meigs, YA Meng, TH Mosley, AB Newman, CH Newton-Cheh, DN Paltoo, GJ Papanicolaou, N Patterson, WS Post, BM Psaty, AN Qasim, L Qu, DJ Rader, S Redline, MP Reilly, AP Reiner, SS Rich, JI Rotter, Y Liu, P Shrader, DS Siscovick, WH Tang, HA Taylor, RP Tracy, RS Vasan, KM Waters, R Wilks, JG Wilson, RR Fabsitz, SB Gabriel, S Kathiresan, E Boerwinkle
Publication Date: 2011-02-10

Variant appearance in text: rs7499892
PubMed Link: 21347282
Variant Present in the following documents:
  • pgen.1001300.s017.doc
View BVdb publication page



Dense genotyping of candidate gene loci identifies variants associated with high-density lipoprotein cholesterol.

Circulation. Cardiovascular Genetics
AC Edmondson, PS Braund, IM Stylianou, AV Khera, CP Nelson, ML Wolfe, SL Derohannessian, BJ Keating, L Qu, J He, MD Tobin, M Tomaszewski, J Baumert, N Klopp, A Döring, B Thorand, M Li, MP Reilly, W Koenig, NJ Samani, DJ Rader
Publication Date: 2011-04

Variant appearance in text: rs7499892
PubMed Link: 21303902
Variant Present in the following documents:
  • NIHMS280051-supplement-1.pdf
View BVdb publication page



Physical activity modifies the effect of LPL, LIPC, and CETP polymorphisms on HDL-C levels and the risk of myocardial infarction in women of European ancestry.

Circulation. Cardiovascular Genetics
T Ahmad, DI Chasman, JE Buring, IM Lee, PM Ridker, BM Everett
Publication Date: 2011-02

Variant appearance in text: rs7499892
PubMed Link: 21252145
Variant Present in the following documents:
  • NIHMS260598-supplement-Supplemental.doc
View BVdb publication page



Genetic causes of high and low serum HDL-cholesterol.

Journal Of Lipid Research
D Weissglas-Volkov, P Pajukanta
Publication Date: 2010-08

Variant appearance in text: rs7499892
PubMed Link: 20421590
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association of lipid-lowering response to statins in combined study populations.

Plos One
MJ Barber, LM Mangravite, CL Hyde, DI Chasman, JD Smith, CA McCarty, X Li, RA Wilke, MJ Rieder, PT Williams, PM Ridker, A Chatterjee, JI Rotter, DA Nickerson, M Stephens, RM Krauss
Publication Date: 2010-03-22

Variant appearance in text: rs7499892
PubMed Link: 20339536
Variant Present in the following documents:
  • pone.0009763.s005.xls
  • pone.0009763.s007.xls
View BVdb publication page



Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study.

Circulation. Cardiovascular Genetics
PM Ridker, G Paré, AN Parker, RY Zee, JP Miletich, DI Chasman
Publication Date: 2009-02

Variant appearance in text: rs7499892
PubMed Link: 20031564
Variant Present in the following documents:
  • Main text
View BVdb publication page



Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.

Plos Genetics
DI Chasman, G Paré, S Mora, JC Hopewell, G Peloso, R Clarke, LA Cupples, A Hamsten, S Kathiresan, A Mälarstig, JM Ordovas, S Ripatti, AN Parker, JP Miletich, PM Ridker
Publication Date: 2009-11

Variant appearance in text: rs7499892
PubMed Link: 19936222
Variant Present in the following documents:
  • pgen.1000730.s004.pdf
  • pgen.1000730.s005.doc
  • pgen.1000730.s007.doc
  • pgen.1000730.s008.doc
View BVdb publication page



Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.

American Journal Of Human Genetics
PJ Talmud, F Drenos, S Shah, T Shah, J Palmen, C Verzilli, TR Gaunt, J Pallas, R Lovering, K Li, JP Casas, R Sofat, M Kumari, S Rodriguez, T Johnson, SJ Newhouse, A Dominiczak, NJ Samani, M Caulfield, P Sever, A Stanton, DC Shields, S Padmanabhan, O Melander, C Hastie, C Delles, S Ebrahim, MG Marmot, GD Smith, DA Lawlor, PB Munroe, IN Day, M Kivimaki, J Whittaker, SE Humphries, AD Hingorani, , ,
Publication Date: 2009-11

Variant appearance in text: rs7499892
PubMed Link: 19913121
Variant Present in the following documents:
  • mmc1.pdf
  • mmc2.xls
View BVdb publication page



Genome-wide association study of biochemical traits in Korcula Island, Croatia.

Croatian Medical Journal
T Zemunik, M Boban, G Lauc, S Janković, K Rotim, Z Vatavuk, G Bencić, Z Dogas, V Boraska, V Torlak, J Susac, I Zobić, D Rudan, D Pulanić, D Modun, I Mudnić, G Gunjaca, D Budimir, C Hayward, V Vitart, AF Wright, H Campbell, I Rudan
Publication Date: 2009-02

Variant appearance in text: rs7499892
PubMed Link: 19260141
Variant Present in the following documents:
  • Main text
View BVdb publication page



Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.

Nature Genetics
YS Aulchenko, S Ripatti, I Lindqvist, D Boomsma, IM Heid, PP Pramstaller, BW Penninx, AC Janssens, JF Wilson, T Spector, NG Martin, NL Pedersen, KO Kyvik, J Kaprio, A Hofman, NB Freimer, MR Jarvelin, U Gyllensten, H Campbell, I Rudan, A Johansson, F Marroni, C Hayward, V Vitart, I Jonasson, C Pattaro, A Wright, N Hastie, I Pichler, AA Hicks, M Falchi, G Willemsen, JJ Hottenga, EJ de Geus, GW Montgomery, J Whitfield, P Magnusson, J Saharinen, M Perola, K Silander, A Isaacs, EJ Sijbrands, AG Uitterlinden, JC Witteman, BA Oostra, P Elliott, A Ruokonen, C Sabatti, C Gieger, T Meitinger, F Kronenberg, A Döring, HE Wichmann, JH Smit, MI McCarthy, CM van Duijn, L Peltonen,
Publication Date: 2009-01

Variant appearance in text: rs7499892
PubMed Link: 19060911
Variant Present in the following documents:
  • NIHMS4347-supplement-figures_and_ta.pdf
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000200676.3 c.750+595C>T - intron_variant - 8/15
ENST00000379780.2 c.750+595C>T - intron_variant - 8/14
ENST00000566128.1 c.555+595C>T - intron_variant - 8/15
ENST00000569082.1 n.852+595C>T - intron_variant,non_coding_transcript_variant - 8/8
NM_000078.3 c.750+595C>T - intron_variant - 8/15
NM_001286085.2 c.750+595C>T - intron_variant - 8/14