Variant ID: 2-21232195-G-A

NM_000384.2(APOB):c.7545C>T;(p.Thr2515Thr)

This variant was identified in 153 publications




Publications:


Influence of multiple apolipoprotein A-I and B genetic variations on insulin resistance and metabolic syndrome in obstructive sleep apnea.

Nutrition & Metabolism
X Li, Z Fu, H Xu, J Zou, H Zhu, Z Li, K Su, Huai, H Yi, J Guan, S Yin
Publication Date: 2020

Variant appearance in text: rs693
PubMed Link: 33005209
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association between apolipoprotein B XbaI polymorphisms and coronary heart disease: A meta-analysis.

Bmc Cardiovascular Disorders
YY Feng, LY Chen, Y Liu, M Luo, TT Yang, YH Hu, J Chang, M Mao
Publication Date: 2020-06-03

Variant appearance in text: rs693
PubMed Link: 32493216
Variant Present in the following documents:
  • Main text
View BVdb publication page



High levels of chemerin associated with variants in the NOS3 and APOB genes in rural populations of Ouro Preto, Minas Gerais, Brazil.

Brazilian Journal Of Medical And Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
AP Batista, KF Barbosa, CZ Masioli, EM Queiroz, CC Marinho, APC Cândido, GLL Machado-Coelho
Publication Date: 2020

Variant appearance in text: rs693
PubMed Link: 32401924
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic Polymorphisms, Mediterranean Diet and Microbiota-Associated Urolithin Metabotypes can Predict Obesity in Childhood-Adolescence.

Scientific Reports
A Cortés-Martín, G Colmenarejo, MV Selma, JC Espín
Publication Date: 2020-05-12

Variant appearance in text: rs693
PubMed Link: 32398726
Variant Present in the following documents:
  • Main text
View BVdb publication page



Distribution of polymorphism rs693 of ApoB gene in a sample of Colombian Caribbeans.

Colombia Medica (Cali, Colombia)
E Mendoza-Torres, NS Pereira Sanandrés, JL Villarreal Camacho, X Mendoza Sánchez, C De La Espriella Pérez, LL Varela Prieto, DA Villanueva Torregrosa
Publication Date: 2019-09-30

Variant appearance in text: rs693
PubMed Link: 32284661
Variant Present in the following documents:
  • Main text
View BVdb publication page



Impact of genetic variants of ABCB1, APOB, CAV1, and NAMPT on susceptibility to pancreatic ductal adenocarcinoma in Chinese patients.

Molecular Genetics & Genomic Medicine
B Li, C Zhang, J Wang, M Zhang, C Liu, Z Chen
Publication Date: 2020-06

Variant appearance in text: rs693
PubMed Link: 32243098
Variant Present in the following documents:
  • Main text
View BVdb publication page



The APOB rs693 polymorphism impacts the lipid profile of Brazilian older adults.

Brazilian Journal Of Medical And Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
ES Alves, AD Henriques, AC Tonet-Furioso, RS Paula, LO Gomes, CF Moraes, OT Nóbrega
Publication Date: 2020

Variant appearance in text: rs693
PubMed Link: 32130292
Variant Present in the following documents:
  • Main text
View BVdb publication page



Quantile-dependent expressivity of postprandial lipemia.

Plos One
PT Williams
Publication Date: 2020

Variant appearance in text: rs693
PubMed Link: 32101585
Variant Present in the following documents:
  • Main text
View BVdb publication page



Utility of genetic variants to predict prognosis in coronary artery disease patients receiving statin treatment.

International Journal Of Clinical And Experimental Pathology
L Zhu, X Ji, L Jiang, Y Zhu, Y Xu, Q Jiang, J Bao, J Ye, H Sheng, H Yu
Publication Date: 2017

Variant appearance in text: rs693
PubMed Link: 31966745
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic risk scores to predict the prognosis of chronic heart failure patients in Chinese Han.

Journal Of Cellular And Molecular Medicine
S Li, Y Sun, S Hu, D Hu, C Li, L Xiao, Y Chen, H Li, G Cui, DW Wang
Publication Date: 2020-01

Variant appearance in text: rs693
PubMed Link: 31670483
Variant Present in the following documents:
  • JCMM-24-285-s001.doc
View BVdb publication page



Tolerability and Safety of a Nutritional Supplement with Potential as Adjuvant in Colorectal Cancer Therapy: A Randomized Trial in Healthy Volunteers.

Nutrients
M Gómez de Cedrón, JM Laparra, V Loria-Kohen, S Molina, J Moreno-Rubio, JJ Montoya, C Torres, E Casado, G Reglero, A Ramírez de Molina
Publication Date: 2019-08-24

Variant appearance in text: rs693
PubMed Link: 31450563
Variant Present in the following documents:
  • nutrients-11-02001-s001.pdf
View BVdb publication page



Exome sequencing of Finnish isolates enhances rare-variant association power.

Nature
AE Locke, KM Steinberg, CWK Chiang, SK Service, AS Havulinna, L Stell, M Pirinen, HJ Abel, CC Chiang, RS Fulton, AU Jackson, CJ Kang, KL Kanchi, DC Koboldt, DE Larson, J Nelson, TJ Nicholas, A Pietilä, V Ramensky, D Ray, LJ Scott, HM Stringham, J Vangipurapu, R Welch, P Yajnik, X Yin, JG Eriksson, M Ala-Korpela, MR Järvelin, M Männikkö, H Laivuori, , SK Dutcher, NO Stitziel, RK Wilson, IM Hall, C Sabatti, A Palotie, V Salomaa, M Laakso, S Ripatti, M Boehnke, NB Freimer
Publication Date: 2019-08

Variant appearance in text: rs693
PubMed Link: 31367044
Variant Present in the following documents:
  • EMS83607-supplement-Supplementary_Tables.xlsx
View BVdb publication page



APOB gene polymorphisms may affect the risk of minor or minimal bleeding complications in patients on warfarin maintaining therapeutic INR.

European Journal Of Human Genetics : Ejhg
J Yee, W Kim, BC Chang, JE Chung, KE Lee, HS Gwak
Publication Date: 2019-10

Variant appearance in text: APOB: 7545C>T; Thr2515=; rs693
PubMed Link: 31186542
Variant Present in the following documents:
  • Main text
View BVdb publication page



Multiple rare and common variants in APOB gene locus associated with oxidatively modified low-density lipoprotein levels.

Plos One
E Khlebus, V Kutsenko, A Meshkov, A Ershova, A Kiseleva, A Shevtsov, N Shcherbakova, A Zharikova, V Lankin, A Tikhaze, I Chazova, E Yarovaya, O Drapkina, S Boytsov
Publication Date: 2019

Variant appearance in text: APOB: Thr2515Thr; rs693
PubMed Link: 31150472
Variant Present in the following documents:
  • Main text
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: rs693
PubMed Link: 31132756
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association between genetic polymorphisms and osteonecrosis in steroid treatment populations: a detailed stratified and dose-response meta-analysis.

Bioscience Reports
J Yang, M Jing, X Yang
Publication Date: 2019-05-31

Variant appearance in text: rs693
PubMed Link: 30996113
Variant Present in the following documents:
  • Main text
View BVdb publication page



Apolipoprotein profiling as a personalized approach to the diagnosis and treatment of dyslipidaemia.

Annals Of Clinical Biochemistry
L Renee Ruhaak, A van der Laarse, CM Cobbaert
Publication Date: 2019-05

Variant appearance in text: rs693
PubMed Link: 30889974
Variant Present in the following documents:
  • 10.1177_0004563219827620.pdf
  • aaaaaMain text
View BVdb publication page



Genetic Identification for Non-Communicable Disease: Findings from 20 Years of the Tehran Lipid and Glucose Study.

International Journal Of Endocrinology And Metabolism
MS Daneshpour, M Hedayati, B Sedaghati-Khayat, K Guity, M Zarkesh, M Akbarzadeh, N Javanrooh, A Zadeh-Vakili, F Azizi
Publication Date: 2018-10

Variant appearance in text: rs693
PubMed Link: 30584432
Variant Present in the following documents:
  • Main text
View BVdb publication page



Lipid Transporter Activity-Related Genetic Polymorphisms Are Associated With Steroid-Induced Osteonecrosis of the Femoral Head: An Updated Meta-Analysis Based on the GRADE Guidelines.

Frontiers In Physiology
X Chen, L Zhang, D Liang, J Li, F Liu, H Ma
Publication Date: 2018

Variant appearance in text: rs693
PubMed Link: 30559675
Variant Present in the following documents:
  • Main text
View BVdb publication page



Vitamin E Metabolic Effects and Genetic Variants: A Challenge for Precision Nutrition in Obesity and Associated Disturbances.

Nutrients
S Galmés, F Serra, A Palou
Publication Date: 2018-12-04

Variant appearance in text: rs693
PubMed Link: 30518135
Variant Present in the following documents:
  • Main text
View BVdb publication page



The Study of rs693 and rs515135 in APOB in People with Familial Hypercholestrolemia.

Cell Journal
F Karami, I Salahshourifar, M Houshmand
Publication Date: 2019-04

Variant appearance in text: rs693
PubMed Link: 30507093
Variant Present in the following documents:
  • Main text
View BVdb publication page



Epigenome wide association study of SNP-CpG interactions on changes in triglyceride levels after pharmaceutical intervention: a GAW20 analysis.

Bmc Proceedings
J Veenstra, A Kalsbeek, K Koster, N Ryder, A Bos, J Huisman, L VanderBerg, J VanderWoude, NL Tintle
Publication Date: 2018

Variant appearance in text: rs693
PubMed Link: 30275900
Variant Present in the following documents:
  • Main text
View BVdb publication page



Improving Imputation Accuracy by Inferring Causal Variants in Genetic Studies.

Journal Of Computational Biology : A Journal Of Computational Molecular Cell Biology
Y Wu, F Hormozdiari, JWJ Joo, E Eskin
Publication Date: 2019-11

Variant appearance in text: rs693
PubMed Link: 30272994
Variant Present in the following documents:
  • Main text
View BVdb publication page



The relationship between apolipoprotein genes polymorphisms and susceptibility to osteonecrosis of the femoral head: a meta-analysis.

Lipids In Health And Disease
Y Hao, H Guo, Z Xu, H Qi, Y Wang, C Lu, J Liu, P Yuan
Publication Date: 2018-08-17

Variant appearance in text: rs693
PubMed Link: 30119683
Variant Present in the following documents:
  • Main text
View BVdb publication page



Global genetic diversity of human apolipoproteins and effects on cardiovascular disease risk.

Journal Of Lipid Research
Y Zhou, R Mägi, L Milani, VM Lauschke
Publication Date: 2018-10

Variant appearance in text: APOB: T2515T; rs693
PubMed Link: 30076208
Variant Present in the following documents:
  • Main text
View BVdb publication page



GWAS Reveal Targets in Vessel Wall Pathways to Treat Coronary Artery Disease.

Frontiers In Cardiovascular Medicine
AW Turner, D Wong, CN Dreisbach, CL Miller
Publication Date: 2018

Variant appearance in text: rs693
PubMed Link: 29988570
Variant Present in the following documents:
  • Main text
View BVdb publication page



Apolipoprotein B and angiotensin-converting enzyme polymorphisms and aerobic interval training: randomized controlled trial in coronary artery disease patients.

Brazilian Journal Of Medical And Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
NY Tamburus, R Verlengia, VC Kunz, MC César, E Silva
Publication Date: 2018

Variant appearance in text: rs693
PubMed Link: 29846435
Variant Present in the following documents:
  • 6944.pdf
  • aaaaaMain text
View BVdb publication page



Emerging Role of Precision Medicine in Cardiovascular Disease.

Circulation Research
JA Leopold, J Loscalzo
Publication Date: 2018-04-27

Variant appearance in text: rs693
PubMed Link: 29700074
Variant Present in the following documents:
  • Main text
View BVdb publication page



Fuzzy set-based generalized multifactor dimensionality reduction analysis of gene-gene interactions.

Bmc Medical Genomics
HY Jung, S Leem, T Park
Publication Date: 2018-04-20

Variant appearance in text: rs693
PubMed Link: 29697366
Variant Present in the following documents:
  • Main text
View BVdb publication page



From SNPs to pathways: Biological interpretation of type 2 diabetes (T2DM) genome wide association study (GWAS) results.

Plos One
E Cirillo, M Kutmon, M Gonzalez Hernandez, T Hooimeijer, ME Adriaens, LMT Eijssen, LD Parnell, SL Coort, CT Evelo
Publication Date: 2018

Variant appearance in text: rs693
PubMed Link: 29617380
Variant Present in the following documents:
  • Main text
  • pone.0193515.s007.xlsx
  • pone.0193515.s008.xlsx
View BVdb publication page



Association between apolipoprotein B genetic polymorphism and the risk of calcific aortic stenosis in Chinese subjects, in Xinjiang, China.

Lipids In Health And Disease
YT Wang, Y Li, YT Ma, YN Yang, X Ma, XM Li, F Liu, BD Chen
Publication Date: 2018-03-07

Variant appearance in text: rs693
PubMed Link: 29514644
Variant Present in the following documents:
  • Main text
View BVdb publication page



Variants in the APOB gene was associated with Ischemic Stroke susceptibility in Chinese Han male population.

Oncotarget
F Zhou, T Guo, L Zhou, Y Zhou, D Yu
Publication Date: 2018-01-05

Variant appearance in text: rs693
PubMed Link: 29416768
Variant Present in the following documents:
  • Main text
View BVdb publication page



APOB codon 4311 polymorphism is associated with hepatitis C virus infection through altered lipid metabolism.

Bmc Gastroenterology
R Harada, M Kimura, Y Sato, T Taniguchi, T Tomonari, T Tanaka, H Tanaka, N Muguruma, H Shinomiya, H Honda, I Imoto, M Sogabe, T Okahisa, T Takayama
Publication Date: 2018-01-30

Variant appearance in text: rs693
PubMed Link: 29382324
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of rs662799 in APOA5 with CAD in Chinese Han population.

Bmc Cardiovascular Disorders
H Chen, S Ding, M Zhou, X Wu, X Liu, Y Wu, D Liu
Publication Date: 2018-01-08

Variant appearance in text: rs693
PubMed Link: 29310573
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide admixture and association study of subclinical atherosclerosis in the Women's Interagency HIV Study (WIHS).

Plos One
A Shendre, HW Wiener, MR Irvin, BE Aouizerat, ET Overton, J Lazar, C Liu, HN Hodis, NA Limdi, KM Weber, SJ Gange, D Zhi, MA Floris-Moore, I Ofotokun, Q Qi, DB Hanna, RC Kaplan, S Shrestha
Publication Date: 2017

Variant appearance in text: rs693
PubMed Link: 29206233
Variant Present in the following documents:
  • pone.0188725.s007.xlsx
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: rs693
PubMed Link: 29084231
Variant Present in the following documents:
  • pgen.1007079.s010.xlsx
  • pgen.1007079.s011.xlsx
View BVdb publication page



Population-based Study of Risk Polymorphisms Associated with Vascular Disorders and Dementia.

Current Genomics
Ó Teijido, JC Carril, R Cacabelos
Publication Date: 2017-10

Variant appearance in text: rs693
PubMed Link: 29081698
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic Risk Factors in Cerebrovascular Disorders and Cognitive Deterioration.

Current Genomics
JC Carril, R Cacabelos
Publication Date: 2017-10

Variant appearance in text: APOB: 7545C>T; Thr2515=; rs693
PubMed Link: 29081697
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association analysis of APO gene polymorphisms with ischemic stroke risk: a case-control study in a Chinese Han population.

Oncotarget
R Xiao, S Sun, J Zhang, Y Ouyang, N Zhang, M Yang, T Jin, Y Xia
Publication Date: 2017-09-01

Variant appearance in text: rs693
PubMed Link: 28947988
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: rs693
PubMed Link: 28875524
Variant Present in the following documents:
  • Main text
  • NIHMS898446-supplement-Supp_TableS1-2.docx
View BVdb publication page



Associations of the APOB rs693 and rs17240441 polymorphisms with plasma APOB and lipid levels: a meta-analysis.

Lipids In Health And Disease
C Niu, Z Luo, L Yu, Y Yang, Y Chen, X Luo, F Lai, Y Song
Publication Date: 2017-09-06

Variant appearance in text: rs693
PubMed Link: 28874158
Variant Present in the following documents:
  • 12944_2017_558_MOESM1_ESM.doc
  • aaaaaMain text
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: rs693
PubMed Link: 28795114
Variant Present in the following documents:
  • Main text
View BVdb publication page



SNPs, linkage disequilibrium, and chronic mountain sickness in Tibetan Chinese.

Hypoxia (Auckland, N.Z.)
NE Buroker, XH Ning, ZN Zhou, K Li, WJ Cen, XF Wu, WZ Zhu, CR Scott, SH Chen
Publication Date: 2017

Variant appearance in text: APOB: 7545C>T; Thr2515Thr; rs693
PubMed Link: 28770234
Variant Present in the following documents:
  • Main text
View BVdb publication page



Gallbladder cancer epidemiology, pathogenesis and molecular genetics: Recent update.

World Journal Of Gastroenterology
A Sharma, KL Sharma, A Gupta, A Yadav, A Kumar
Publication Date: 2017-06-14

Variant appearance in text: rs693
PubMed Link: 28652652
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic determinants of inherited susceptibility to hypercholesterolemia - a comprehensive literature review.

Lipids In Health And Disease
CS Paththinige, ND Sirisena, V Dissanayake
Publication Date: 2017-06-02

Variant appearance in text: rs693
PubMed Link: 28577571
Variant Present in the following documents:
  • 12944_2017_488_MOESM1_ESM.xlsx
  • aaaaaMain text
View BVdb publication page



GRECOS Project (Genotyping Recurrence Risk of Stroke): The Use of Genetics to Predict the Vascular Recurrence After Stroke.

Stroke
I Fernández-Cadenas, M Mendióroz, D Giralt, C Nafria, E Garcia, C Carrera, C Gallego-Fabrega, S Domingues-Montanari, P Delgado, M Ribó, M Castellanos, S Martínez, M Freijo, J Jiménez-Conde, M Rubiera, J Alvarez-Sabín, CA Molina, MA Font, M Grau Olivares, E Palomeras, N Perez de la Ossa, M Martinez-Zabaleta, J Masjuan, F Moniche, D Canovas, C Piñana, F Purroy, D Cocho, I Navas, C Tejero, N Aymerich, N Cullell, E Muiño, J Serena, F Rubio, A Davalos, J Roquer, JF Arenillas, J Martí-Fábregas, K Keene, WM Chen, B Worrall, M Sale, A Arboix, J Krupinski, J Montaner,
Publication Date: 2017-05

Variant appearance in text: rs693
PubMed Link: 28411264
Variant Present in the following documents:
  • NIHMS861713-supplement-Supplemental_Material.pdf
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: rs693
PubMed Link: 28270201
Variant Present in the following documents:
  • 13073_2017_414_MOESM11_ESM.xlsx
View BVdb publication page



Genetic Regulation of Adipose Gene Expression and Cardio-Metabolic Traits.

American Journal Of Human Genetics
M Civelek, Y Wu, C Pan, CK Raulerson, A Ko, A He, C Tilford, NK Saleem, A Stančáková, LJ Scott, C Fuchsberger, HM Stringham, AU Jackson, N Narisu, PS Chines, KS Small, J Kuusisto, BW Parks, P Pajukanta, T Kirchgessner, FS Collins, PS Gargalovic, M Boehnke, M Laakso, KL Mohlke, AJ Lusis
Publication Date: 2017-03-02

Variant appearance in text: rs693
PubMed Link: 28257690
Variant Present in the following documents:
  • mmc3.xlsx
View BVdb publication page



Apolipoprotein B Gene Polymorphisms and Dyslipidemia in HIV Infected Adult Zimbabweans.

The Open Aids Journal
V Kodogo, DT Zhou, O Oektedalen, K Duri, B Stray-Pedersen, E Gomo
Publication Date: 2016

Variant appearance in text: rs693
PubMed Link: 27790293
Variant Present in the following documents:
  • Main text
View BVdb publication page



Uncoupling associations of risk alleles with endophenotypes and phenotypes: insights from the ApoB locus and heart-related traits.

Aging Cell
AM Kulminski, Y Kernogitski, I Culminskaya, Y Loika, KG Arbeev, O Bagley, M Duan, L Arbeeva, SV Ukraintseva, D Wu, E Stallard, AI Yashin
Publication Date: 2017-02

Variant appearance in text: rs693
PubMed Link: 27683205
Variant Present in the following documents:
  • Main text
  • ACEL-16-61-s002.pdf
  • ACEL-16-61-s003.pdf
  • ACEL-16-61-s004.pdf
  • ACEL-16-61-s005.pdf
  • ACEL-16-61-s006.pdf
  • ACEL-16-61-s007.pdf
  • ACEL-16-61-s008.pdf
  • ACEL-16-61-s009.pdf
  • ACEL-16-61-s010.pdf
  • ACEL-16-61-s011.pdf
  • ACEL-16-61-s012.pdf
View BVdb publication page



Association Between Apolipoprotein B XbaI Polymorphism and Coronary Heart Disease in Han Chinese Population: A Meta-Analysis.

Genetic Testing And Molecular Biomarkers
Y Chen, M Lin, Y Liang, N Zhang, S Rao
Publication Date: 2016-06

Variant appearance in text: rs693
PubMed Link: 27172140
Variant Present in the following documents:
  • Main text
View BVdb publication page



Harnessing publicly available genetic data to prioritize lipid modifying therapeutic targets for prevention of coronary heart disease based on dysglycemic risk.

Human Genetics
V Tragante, FW Asselbergs, DI Swerdlow, TM Palmer, JH Moore, PIW de Bakker, BJ Keating, MV Holmes
Publication Date: 2016-05

Variant appearance in text: rs693
PubMed Link: 26946290
Variant Present in the following documents:
  • Main text
View BVdb publication page



An Adaptive Ridge Procedure for L0 Regularization.

Plos One
F Frommlet, G Nuel
Publication Date: 2016

Variant appearance in text: rs693
PubMed Link: 26849123
Variant Present in the following documents:
  • Main text
View BVdb publication page



Privacy-preserving genomic testing in the clinic: a model using HIV treatment.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
PJ McLaren, JL Raisaro, M Aouri, M Rotger, E Ayday, I Bartha, MB Delgado, Y Vallet, HF Günthard, M Cavassini, H Furrer, T Doco-Lecompte, C Marzolini, P Schmid, C Di Benedetto, LA Decosterd, J Fellay, JP Hubaux, A Telenti
Publication Date: 2016-08

Variant appearance in text: rs693
PubMed Link: 26765343
Variant Present in the following documents:
  • gim2015167x5.doc
  • gim2015167x8.doc
View BVdb publication page



Association between the APOB XbaI and EcoRI polymorphisms and lipids in Chinese: a meta-analysis.

Lipids In Health And Disease
W Gu, M Zhang, S Wen
Publication Date: 2015-10-07

Variant appearance in text: rs693
PubMed Link: 26446158
Variant Present in the following documents:
  • Main text
View BVdb publication page



The APOB gene polymorphism in the pathogenesis of gallstone disease in pre- and postmenopausal women.

Przeglad Menopauzalny = Menopause Review
K Rudzińska, A Bogacz, D Kotrych, H Wolski, M Majchrzycki, A Seremak-Mrozikiewicz, B Kosiński, B Czerny
Publication Date: 2015-03

Variant appearance in text: rs693
PubMed Link: 26327886
Variant Present in the following documents:
  • Main text
View BVdb publication page



Proinflammatory genotype is associated with the frailty phenotype in the English Longitudinal Study of Ageing.

Aging Clinical And Experimental Research
K Mekli, JY Nazroo, AD Marshall, M Kumari, N Pendleton
Publication Date: 2016-06

Variant appearance in text: rs693
PubMed Link: 26248682
Variant Present in the following documents:
  • 40520_2015_419_MOESM2_ESM.xlsx
View BVdb publication page



Evaluation of transethnic fine mapping with population-specific and cosmopolitan imputation reference panels in diverse Asian populations.

European Journal Of Human Genetics : Ejhg
X Wang, CY Cheng, J Liao, X Sim, J Liu, KS Chia, ES Tai, P Little, CC Khor, T Aung, TY Wong, YY Teo
Publication Date: 2016-04

Variant appearance in text: rs693
PubMed Link: 26130488
Variant Present in the following documents:
  • ejhg2015150x4.xls
View BVdb publication page



Apolipoprotein E and protection against hepatitis E viral infection in American non-Hispanic blacks.

Hepatology (Baltimore, Md.)
L Zhang, A Yesupriya, MH Chang, E Teshale, CG Teo
Publication Date: 2015-11

Variant appearance in text: rs693
PubMed Link: 26096528
Variant Present in the following documents:
  • NIHMS1043972-supplement-Supplemental.pdf
View BVdb publication page



AllelicImbalance: an R/bioconductor package for detecting, managing, and visualizing allele expression imbalance data from RNA sequencing.

Bmc Bioinformatics
JR Gådin, FM van't Hooft, P Eriksson, L Folkersen
Publication Date: 2015-06-12

Variant appearance in text: rs693
PubMed Link: 26066318
Variant Present in the following documents:
  • 12859_2015_620_MOESM1_ESM.pdf
View BVdb publication page



Detection of pleiotropy through a Phenome-wide association study (PheWAS) of epidemiologic data as part of the Environmental Architecture for Genes Linked to Environment (EAGLE) study.

Plos Genetics
MA Hall, A Verma, KD Brown-Gentry, R Goodloe, J Boston, S Wilson, B McClellan, C Sutcliffe, HH Dilks, NB Gillani, H Jin, P Mayo, M Allen, N Schnetz-Boutaud, DC Crawford, MD Ritchie, SA Pendergrass
Publication Date: 2014-12

Variant appearance in text: rs693
PubMed Link: 25474351
Variant Present in the following documents:
  • pgen.1004678.s007.xlsx
View BVdb publication page



The challenges of genome-wide interaction studies: lessons to learn from the analysis of HDL blood levels.

Plos One
EM van Leeuwen, FA Smouter, T Kam-Thong, N Karbalai, AV Smith, TB Harris, LJ Launer, CM Sitlani, G Li, JA Brody, JC Bis, CC White, A Jaiswal, BA Oostra, A Hofman, F Rivadeneira, AG Uitterlinden, E Boerwinkle, CM Ballantyne, V Gudnason, BM Psaty, LA Cupples, MR Järvelin, S Ripatti, A Isaacs, B Müller-Myhsok, LC Karssen, CM van Duijn
Publication Date: 2014

Variant appearance in text: rs693
PubMed Link: 25329471
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic association of APOB polymorphisms with variation in serum lipid profile among the Kuwait population.

Lipids In Health And Disease
SA Al-Bustan, MA Alnaqeeb, BG Annice, GA Ebrahim, TM Refai
Publication Date: 2014-10-08

Variant appearance in text: rs693
PubMed Link: 25292352
Variant Present in the following documents:
  • 12944_2014_1139_MOESM1_ESM.pdf
  • 12944_2014_1139_MOESM2_ESM.doc
  • 12944_2014_1139_MOESM3_ESM.docx
  • aaaaaMain text
View BVdb publication page



Identification of genes contributing to cardiovascular disease in overweight and obese individuals from West Virginia.

The West Virginia Medical Journal
Y Dementieva, TL Green, DA Primerano, L Wei, J Denvir, P Wehner, S Dodson, MR Flood, BA Pollock, M Huff, C Hill, R Kreisberg, A Francis, K Morrison, H Blackwood, M Davis, HM Lee, S Warren,
Publication Date: 2012

Variant appearance in text: rs693
PubMed Link: 25134189
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of genetic variants with rapid fibrosis: progression after liver transplantation for hepatitis C.

Transplantation
JE Layden, BO Tayo, SJ Cotler, NM Clark, K Baraoidan, SL Friedman, RS Cooper
Publication Date: 2014-05-27

Variant appearance in text: rs693
PubMed Link: 24770613
Variant Present in the following documents:
  • Main text
  • NIHMS710967-supplement-Supplemental_file.pdf
View BVdb publication page



Multiancestral analysis of inflammation-related genetic variants and C-reactive protein in the population architecture using genomics and epidemiology study.

Circulation. Cardiovascular Genetics
JM Kocarnik, SA Pendergrass, CL Carty, JS Pankow, FR Schumacher, I Cheng, P Durda, JL Ambite, E Deelman, NR Cook, S Liu, J Wactawski-Wende, C Hutter, K Brown-Gentry, S Wilson, LG Best, N Pankratz, CP Hong, SA Cole, VS Voruganti, P Bůžkova, NW Jorgensen, NS Jenny, LR Wilkens, CA Haiman, LN Kolonel, A Lacroix, K North, R Jackson, L Le Marchand, LA Hindorff, DC Crawford, M Gross, U Peters
Publication Date: 2014-04

Variant appearance in text: rs693
PubMed Link: 24622110
Variant Present in the following documents:
  • NIHMS575195-supplement-000173_-_Supplemental_Material.pdf
View BVdb publication page



A genome wide association study identifies common variants associated with lipid levels in the Chinese population.

Plos One
L Zhou, M He, Z Mo, C Wu, H Yang, D Yu, X Yang, X Zhang, Y Wang, J Sun, Y Gao, A Tan, Y He, H Zhang, X Qin, J Zhu, H Li, X Lin, J Zhu, X Min, M Lang, D Li, K Zhai, J Chang, W Tan, J Yuan, W Chen, Y Wang, S Wei, X Miao, F Wang, W Fang, Y Liang, Q Deng, X Dai, D Lin, S Huang, H Guo, S Lilly Zheng, J Xu, D Lin, FB Hu, T Wu
Publication Date: 2013

Variant appearance in text: rs693
PubMed Link: 24386095
Variant Present in the following documents:
  • Main text
  • pone.0082420.s002.doc
View BVdb publication page



The roles of genetic polymorphisms and human immunodeficiency virus infection in lipid metabolism.

Biomed Research International
ER de Almeida, EM Reiche, AP Kallaur, T Flauzino, MA Watanabe
Publication Date: 2013

Variant appearance in text: rs693
PubMed Link: 24319689
Variant Present in the following documents:
  • Main text
View BVdb publication page



Biobanking across the phenome - at the center of chronic disease research.

Bmc Public Health
M Imboden, NM Probst-Hensch
Publication Date: 2013-11-25

Variant appearance in text: rs693
PubMed Link: 24274136
Variant Present in the following documents:
  • 1471-2458-13-1094-S2.xlsx
View BVdb publication page



Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data.

Nature Biotechnology
JC Denny, L Bastarache, MD Ritchie, RJ Carroll, R Zink, JD Mosley, JR Field, JM Pulley, AH Ramirez, E Bowton, MA Basford, DS Carrell, PL Peissig, AN Kho, JA Pacheco, LV Rasmussen, DR Crosslin, PK Crane, J Pathak, SJ Bielinski, SA Pendergrass, H Xu, LA Hindorff, R Li, TA Manolio, CG Chute, RL Chisholm, EB Larson, GP Jarvik, MH Brilliant, CA McCarty, IJ Kullo, JL Haines, DC Crawford, DR Masys, DM Roden
Publication Date: 2013-12

Variant appearance in text: rs693
PubMed Link: 24270849
Variant Present in the following documents:
  • Main text
  • NIHMS561785-supplement-supplementary_data.pdf
View BVdb publication page



Genetic markers associated to dyslipidemia in HIV-infected individuals on HAART.

Thescientificworldjournal
RK Lazzaretti, AS Gasparotto, MG Sassi, CA Polanczyk, R Kuhmmer, JM Silveira, RP Basso, CA Pinheiro, MF Silveira, E Sprinz, VS Mattevi
Publication Date: 2013

Variant appearance in text: rs693
PubMed Link: 24191141
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic susceptibility for ischemic infarction and arteriolosclerosis based on neuropathologic evaluations.

Cerebrovascular Diseases (Basel, Switzerland)
SY Chou, JM Shulman, BT Keenan, EA Secor, AS Buchman, J Schneider, DA Bennett, PL De Jager
Publication Date: 2013

Variant appearance in text: rs693
PubMed Link: 24135527
Variant Present in the following documents:
  • NIHMS527173-supplement-01.pdf
View BVdb publication page



No evidence of interaction between known lipid-associated genetic variants and smoking in the multi-ethnic PAGE population.

Human Genetics
L Dumitrescu, CL Carty, N Franceschini, LA Hindorff, SA Cole, P Bůžková, FR Schumacher, CB Eaton, RJ Goodloe, DJ Duggan, J Haessler, B Cochran, BE Henderson, I Cheng, KC Johnson, CS Carlson, SA Love, K Brown-Gentry, AQ Nato, M Quibrera, RV Shohet, JL Ambite, LR Wilkens, L Le Marchand, CA Haiman, S Buyske, C Kooperberg, KE North, M Fornage, DC Crawford
Publication Date: 2013-12

Variant appearance in text: rs693
PubMed Link: 24100633
Variant Present in the following documents:
  • NIHMS530028-supplement-439_2013_1375_MOESM1_ESM.docx
View BVdb publication page



Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study.

Plos Biology
CS Carlson, TC Matise, KE North, CA Haiman, MD Fesinmeyer, S Buyske, FR Schumacher, U Peters, N Franceschini, MD Ritchie, DJ Duggan, KL Spencer, L Dumitrescu, CB Eaton, F Thomas, A Young, C Carty, G Heiss, L Le Marchand, DC Crawford, LA Hindorff, CL Kooperberg,
Publication Date: 2013-09

Variant appearance in text: rs693
PubMed Link: 24068893
Variant Present in the following documents:
  • pbio.1001661.s003.xlsx
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000233242.1 c.7545C>T p.Thr2515= synonymous_variant 26/29 -
NM_000384.3 c.7545C>T p.Thr2515= synonymous_variant 26/29 -