Variant ID: 19-45412040-C-T

NM_000041.2(APOE):c.487C>T;(p.R163C)

This variant was identified in 23 publications

View GRCh38 version.




Publications:


APOE Molecular Spectrum in a French Cohort with Primary Dyslipidemia.

International Journal Of Molecular Sciences
Abou Khalil, Yara Y; Marmontel, Oriane O; Ferrières, Jean J; Paillard, François F; Yelnik, Cécile C; Carreau, Valérie V; Charrière, Sybil S; Bruckert, Eric E; Gallo, Antonio A; Giral, Philippe P; Philippi, Anne A; Bluteau, Olivier O; Boileau, Catherine C; Abifadel, Marianne M; Di-Filippo, Mathilde M; Carrié, Alain A; Rabès, Jean-Pierre JP; Varret, Mathilde M
Publication Date: 2022-05-21

Variant appearance in text: APOE: 487C>T; Arg163Cys; rs769455
PubMed Link: 35628605
Variant Present in the following documents:
  • Main text
  • ijms-23-05792.pdf
View BVdb publication page



Answer ALS, a large-scale resource for sporadic and familial ALS combining clinical and multi-omics data from induced pluripotent cell lines.

Nature Neuroscience
Baxi, Emily G EG; Thompson, Terri T; Li, Jonathan J; Kaye, Julia A JA; Lim, Ryan G RG; Wu, Jie J; Ramamoorthy, Divya D; Lima, Leandro L; Vaibhav, Vineet V; Matlock, Andrea A; Frank, Aaron A; Coyne, Alyssa N AN; Landin, Barry B; Ornelas, Loren L; Mosmiller, Elizabeth E; Thrower, Sara S; Farr, S Michelle SM; Panther, Lindsey L; Gomez, Emilda E; Galvez, Erick E; Perez, Daniel D; Meepe, Imara I; Lei, Susan S; Mandefro, Berhan B; Trost, Hannah H; Pinedo, Louis L; Banuelos, Maria G MG; Liu, Chunyan C; Moran, Ruby R; Garcia, Veronica V; Workman, Michael M; Ho, Richie R; Wyman, Stacia S; Roggenbuck, Jennifer J; Harms, Matthew B MB; Stocksdale, Jennifer J; Miramontes, Ricardo R; Wang, Keona K; Venkatraman, Vidya V; Holewenski, Ronald R; Sundararaman, Niveda N; Pandey, Rakhi R; Manalo, Danica-Mae DM; Donde, Aneesh A; Huynh, Nhan N; Adam, Miriam M; Wassie, Brook T BT; Vertudes, Edward E; Amirani, Naufa N; Raja, Krishna K; Thomas, Reuben R; Hayes, Lindsey L; Lenail, Alex A; Cerezo, Aianna A; Luppino, Sarah S; Farrar, Alanna A; Pothier, Lindsay L; Prina, Carolyn C; Morgan, Todd T; Jamil, Arish A; Heintzman, Sarah S; Jockel-Balsarotti, Jennifer J; Karanja, Elizabeth E; Markway, Jesse J; McCallum, Molly M; Joslin, Ben B; Alibazoglu, Deniz D; Kolb, Stephen S; Ajroud-Driss, Senda S; Baloh, Robert R; Heitzman, Daragh D; Miller, Tim T; Glass, Jonathan D JD; Patel-Murray, Natasha Leanna NL; Yu, Hong H; Sinani, Ervin E; Vigneswaran, Prasha P; Sherman, Alexander V AV; Ahmad, Omar O; Roy, Promit P; Beavers, Jay C JC; Zeiler, Steven S; Krakauer, John W JW; Agurto, Carla C; Cecchi, Guillermo G; Bellard, Mary M; Raghav, Yogindra Y; Sachs, Karen K; Ehrenberger, Tobias T; Bruce, Elizabeth E; Cudkowicz, Merit E ME; Maragakis, Nicholas N; Norel, Raquel R; Van Eyk, Jennifer E JE; Finkbeiner, Steven S; Berry, James J; Sareen, Dhruv D; Thompson, Leslie M LM; Fraenkel, Ernest E; Svendsen, Clive N CN; Rothstein, Jeffrey D JD
Publication Date: 2022-02-03

Variant appearance in text: APOE: R163C; rs769455
PubMed Link: 35115730
Variant Present in the following documents:
  • 41593_2021_1006_MOESM4_ESM.xlsx
View BVdb publication page



High-depth African genomes inform human migration and health.

Nature
Choudhury, Ananyo A; Aron, Shaun S; Botigué, Laura R LR; Sengupta, Dhriti D; Botha, Gerrit G; Bensellak, Taoufik T; Wells, Gordon G; Kumuthini, Judit J; Shriner, Daniel D; Fakim, Yasmina J YJ; Ghoorah, Anisah W AW; Dareng, Eileen E; Odia, Trust T; Falola, Oluwadamilare O; Adebiyi, Ezekiel E; Hazelhurst, Scott S; Mazandu, Gaston G; Nyangiri, Oscar A OA; Mbiyavanga, Mamana M; Benkahla, Alia A; Kassim, Samar K SK; Mulder, Nicola N; Adebamowo, Sally N SN; Chimusa, Emile R ER; Muzny, Donna D; Metcalf, Ginger G; Gibbs, Richard A RA; , ; Rotimi, Charles C; Ramsay, Michèle M; , ; Adeyemo, Adebowale A AA; Lombard, Zané Z; Hanchard, Neil A NA
Publication Date: 2020-10

Variant appearance in text: APOE: 487C>T; Arg163Cys
PubMed Link: 33116287
Variant Present in the following documents:
  • 41586_2020_2859_MOESM3_ESM.xlsx
View BVdb publication page



Reference exome data for a Northern Brazilian population.

Scientific Data
Weeks, Alexia L AL; Francis, Richard W RW; Neri, Joao I C F JICF; Costa, Nathaly M C NMC; Arrais, Nivea M R NMR; Lassmann, Timo T; Blackwell, Jenefer M JM; Jeronimo, Selma M B SMB
Publication Date: 2020-10-21

Variant appearance in text: APOE: 487C>T; Arg163Cys; rs769455
PubMed Link: 33087711
Variant Present in the following documents:
  • 41597_2020_703_MOESM2_ESM.xlsx
View BVdb publication page



Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study.

Plos Genetics
Hu, Yao Y; Graff, Mariaelisa M; Haessler, Jeffrey J; Buyske, Steven S; Bien, Stephanie A SA; Tao, Ran R; Highland, Heather M HM; Nishimura, Katherine K KK; Zubair, Niha N; Lu, Yingchang Y; Verbanck, Marie M; Hilliard, Austin T AT; Klarin, Derek D; Damrauer, Scott M SM; Ho, Yuk-Lam YL; , ; Wilson, Peter W F PWF; Chang, Kyong-Mi KM; Tsao, Philip S PS; Cho, Kelly K; O'Donnell, Christopher J CJ; Assimes, Themistocles L TL; Petty, Lauren E LE; Below, Jennifer E JE; Dikilitas, Ozan O; Schaid, Daniel J DJ; Kosel, Matthew L ML; Kullo, Iftikhar J IJ; Rasmussen-Torvik, Laura J LJ; Jarvik, Gail P GP; Feng, Qiping Q; Wei, Wei-Qi WQ; Larson, Eric B EB; Mentch, Frank D FD; Almoguera, Berta B; Sleiman, Patrick M PM; Raffield, Laura M LM; Correa, Adolfo A; Martin, Lisa W LW; Daviglus, Martha M; Matise, Tara C TC; Ambite, Jose Luis JL; Carlson, Christopher S CS; Do, Ron R; Loos, Ruth J F RJF; Wilkens, Lynne R LR; Le Marchand, Loic L; Haiman, Chris C; Stram, Daniel O DO; Hindorff, Lucia A LA; North, Kari E KE; Kooperberg, Charles C; Cheng, Iona I; Peters, Ulrike U
Publication Date: 2020-03

Variant appearance in text: rs769455
PubMed Link: 32226016
Variant Present in the following documents:
  • Main text
View BVdb publication page



Apolipoprotein E-C1-C4-C2 gene cluster region and inter-individual variation in plasma lipoprotein levels: a comprehensive genetic association study in two ethnic groups.

Plos One
Pirim, Dilek D; Radwan, Zaheda H ZH; Wang, Xingbin X; Niemsiri, Vipavee V; Hokanson, John E JE; Hamman, Richard F RF; Feingold, Eleanor E; Bunker, Clareann H CH; Demirci, F Yesim FY; Kamboh, M Ilyas MI
Publication Date: 2019

Variant appearance in text: APOE: Arg163Cys; rs769455
PubMed Link: 30913229
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
Zhou, Yitian Y; Mägi, Reedik R; Milani, Lili L; Lauschke, Volker M VM
Publication Date: 2018-10

Variant appearance in text: APOE: R163C; rs769455
PubMed Link: 30076208
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project.

Dementia And Geriatric Cognitive Disorders
Blue, Elizabeth E EE; Bis, Joshua C JC; Dorschner, Michael O MO; Tsuang, Debby W DW; Barral, Sandra M SM; Beecham, Gary G; Below, Jennifer E JE; Bush, William S WS; Butkiewicz, Mariusz M; Cruchaga, Carlos C; DeStefano, Anita A; Farrer, Lindsay A LA; Goate, Alison A; Haines, Jonathan J; Jaworski, Jim J; Jun, Gyungah G; Kunkle, Brian B; Kuzma, Amanda A; Lee, Jenny J JJ; Lunetta, Kathryn L KL; Ma, Yiyi Y; Martin, Eden E; Naj, Adam A; Nato, Alejandro Q AQ; Navas, Patrick P; Nguyen, Hiep H; Reitz, Christiane C; Reyes, Dolly D; Salerno, William W; Schellenberg, Gerard D GD; Seshadri, Sudha S; Sohi, Harkirat H; Thornton, Timothy A TA; Valadares, Otto O; van Duijn, Cornelia C; Vardarajan, Badri N BN; Wang, Li-San LS; Boerwinkle, Eric E; Dupuis, Josée J; Pericak-Vance, Margaret A MA; Mayeux, Richard R; Wijsman, Ellen M EM; ,
Publication Date: 2018

Variant appearance in text: rs769455
PubMed Link: 29486463
Variant Present in the following documents:
  • Main text
View BVdb publication page



In silico analyses of deleterious missense SNPs of human apolipoprotein E3.

Scientific Reports
Pires, Allan S AS; Porto, William F WF; Franco, Octavio L OL; Alencar, Sérgio A SA
Publication Date: 2017-05-30

Variant appearance in text: APOE: Arg163Cys
PubMed Link: 28559539
Variant Present in the following documents:
  • Main text
View BVdb publication page



Evaluation of 10 AMD Associated Polymorphisms as a Cause of Choroidal Neovascularization in Highly Myopic Eyes.

Plos One
Velazquez-Villoria, Alvaro A; Recalde, Sergio S; Anter, Jaouad J; Bezunartea, Jaione J; Hernandez-Sanchez, Maria M; García-García, Laura L; Alonso, Elena E; Ruiz-Moreno, Jose María JM; Araiz-Iribarren, Javier J; Fernandez-Robredo, Patricia P; García-Layana, Alfredo A
Publication Date: 2016

Variant appearance in text: rs769455
PubMed Link: 27643879
Variant Present in the following documents:
  • Main text
View BVdb publication page



Global molecular analysis and APOE mutations in a cohort of autosomal dominant hypercholesterolemia patients in France.

Journal Of Lipid Research
Wintjens, René R; Bozon, Dominique D; Belabbas, Khaldia K; MBou, Félicien F; Girardet, Jean-Philippe JP; Tounian, Patrick P; Jolly, Mathilde M; Boccara, Franck F; Cohen, Ariel A; Karsenty, Alexandra A; Dubern, Béatrice B; Carel, Jean-Claude JC; Azar-Kolakez, Ahlam A; Feillet, François F; Labarthe, François F; Gorsky, Anne-Marie Colin AM; Horovitz, Alice A; Tamarindi, Catherine C; Kieffer, Pierre P; Lienhardt, Anne A; Lascols, Olivier O; Di Filippo, Mathilde M; Dufernez, Fabienne F
Publication Date: 2016-03

Variant appearance in text: APOE: Arg163Cys
PubMed Link: 26802169
Variant Present in the following documents:
  • Main text
View BVdb publication page



INOSA Guidelines in the era of precision medicine.

The Indian Journal Of Medical Research
Chakraborty, Ranajit R
Publication Date: 2015-08

Variant appearance in text: rs769455
PubMed Link: 26354222
Variant Present in the following documents:
  • Main text
View BVdb publication page



Comprehensive evaluation of the association of APOE genetic variation with plasma lipoprotein traits in U.S. whites and African blacks.

Plos One
Radwan, Zaheda H ZH; Wang, Xingbin X; Waqar, Fahad F; Pirim, Dilek D; Niemsiri, Vipavee V; Hokanson, John E JE; Hamman, Richard F RF; Bunker, Clareann H CH; Barmada, M Michael MM; Demirci, F Yesim FY; Kamboh, M Ilyas MI
Publication Date: 2014

Variant appearance in text: APOE: Arg163Cys; rs769455
PubMed Link: 25502880
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of rare variants in Alzheimer's disease.

Frontiers In Genetics
Lord, Jenny J; Lu, Alexander J AJ; Cruchaga, Carlos C
Publication Date: 2014

Variant appearance in text: rs769455
PubMed Link: 25389433
Variant Present in the following documents:
  • Main text
View BVdb publication page



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

Genetic Epidemiology
Hellwege, Jacklyn N JN; Palmer, Nicholette D ND; Raffield, Laura M LM; Ng, Maggie C Y MC; Hawkins, Gregory A GA; Long, Jirong J; Lorenzo, Carlos C; Norris, Jill M JM; Ida Chen, Y-D YD; Speliotes, Elizabeth K EK; Rotter, Jerome I JI; Langefeld, Carl D CD; Wagenknecht, Lynne E LE; Bowden, Donald W DW
Publication Date: 2014-05

Variant appearance in text: APOE: R163C; rs769455
PubMed Link: 24719370
Variant Present in the following documents:
  • Main text
View BVdb publication page



ApoE variant p.V236E is associated with markedly reduced risk of Alzheimer's disease.

Molecular Neurodegeneration
Medway, Christopher W CW; Abdul-Hay, Samer S; Mims, Tynickwa T; Ma, Li L; Bisceglio, Gina G; Zou, Fanggeng F; Pankratz, Shane S; Sando, Sigrid B SB; Aasly, Jan O JO; Barcikowska, Maria M; Siuda, Joanna J; Wszolek, Zbigniew K ZK; Ross, Owen A OA; Carrasquillo, Minerva M; Dickson, Dennis W DW; Graff-Radford, Neill N; Petersen, Ronald C RC; Ertekin-Taner, Nilüfer N; Morgan, Kevin K; Bu, Guojun G; Younkin, Steven G SG
Publication Date: 2014-03-10

Variant appearance in text: rs769455
PubMed Link: 24607147
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.

American Journal Of Human Genetics
Peloso, Gina M GM; Auer, Paul L PL; Bis, Joshua C JC; Voorman, Arend A; Morrison, Alanna C AC; Stitziel, Nathan O NO; Brody, Jennifer A JA; Khetarpal, Sumeet A SA; Crosby, Jacy R JR; Fornage, Myriam M; Isaacs, Aaron A; Jakobsdottir, Johanna J; Feitosa, Mary F MF; Davies, Gail G; Huffman, Jennifer E JE; Manichaikul, Ani A; Davis, Brian B; Lohman, Kurt K; Joon, Aron Y AY; Smith, Albert V AV; Grove, Megan L ML; Zanoni, Paolo P; Redon, Valeska V; Demissie, Serkalem S; Lawson, Kim K; Peters, Ulrike U; Carlson, Christopher C; Jackson, Rebecca D RD; Ryckman, Kelli K KK; Mackey, Rachel H RH; Robinson, Jennifer G JG; Siscovick, David S DS; Schreiner, Pamela J PJ; Mychaleckyj, Josyf C JC; Pankow, James S JS; Hofman, Albert A; Uitterlinden, Andre G AG; Harris, Tamara B TB; Taylor, Kent D KD; Stafford, Jeanette M JM; Reynolds, Lindsay M LM; Marioni, Riccardo E RE; Dehghan, Abbas A; Franco, Oscar H OH; Patel, Aniruddh P AP; Lu, Yingchang Y; Hindy, George G; Gottesman, Omri O; Bottinger, Erwin P EP; Melander, Olle O; Orho-Melander, Marju M; Loos, Ruth J F RJ; Duga, Stefano S; Merlini, Piera Angelica PA; Farrall, Martin M; Goel, Anuj A; Asselta, Rosanna R; Girelli, Domenico D; Martinelli, Nicola N; Shah, Svati H SH; Kraus, William E WE; Li, Mingyao M; Rader, Daniel J DJ; Reilly, Muredach P MP; McPherson, Ruth R; Watkins, Hugh H; Ardissino, Diego D; , ; Zhang, Qunyuan Q; Wang, Judy J; Tsai, Michael Y MY; Taylor, Herman A HA; Correa, Adolfo A; Griswold, Michael E ME; Lange, Leslie A LA; Starr, John M JM; Rudan, Igor I; Eiriksdottir, Gudny G; Launer, Lenore J LJ; Ordovas, Jose M JM; Levy, Daniel D; Chen, Y-D Ida YD; Reiner, Alexander P AP; Hayward, Caroline C; Polasek, Ozren O; Deary, Ian J IJ; Borecki, Ingrid B IB; Liu, Yongmei Y; Gudnason, Vilmundur V; Wilson, James G JG; van Duijn, Cornelia M CM; Kooperberg, Charles C; Rich, Stephen S SS; Psaty, Bruce M BM; Rotter, Jerome I JI; O'Donnell, Christopher J CJ; Rice, Kenneth K; Boerwinkle, Eric E; Kathiresan, Sekar S; Cupples, L Adrienne LA
Publication Date: 2014-02-06

Variant appearance in text: APOE: 487C>T; Arg163Cys; rs769455
PubMed Link: 24507774
Variant Present in the following documents:
  • Main text
View BVdb publication page



Prevalence of the apolipoprotein E Arg145Cys dyslipidemia at-risk polymorphism in African-derived populations.

The American Journal Of Cardiology
Abou Ziki, Maen D MD; Strulovici-Barel, Yael Y; Hackett, Neil R NR; Rodriguez-Flores, Juan L JL; Mezey, Jason G JG; Salit, Jacqueline J; Radisch, Sharon S; Hollmann, Charleen C; Chouchane, Lotfi L; Malek, Joel J; Zirie, Mahmoud A MA; Jayyuosi, Amin A; Gotto, Antonio M AM; Crystal, Ronald G RG
Publication Date: 2014-01-15

Variant appearance in text: rs769455
PubMed Link: 24239320
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
Wu, Ying Y; Waite, Lindsay L LL; Jackson, Anne U AU; Sheu, Wayne H-H WH; Buyske, Steven S; Absher, Devin D; Arnett, Donna K DK; Boerwinkle, Eric E; Bonnycastle, Lori L LL; Carty, Cara L CL; Cheng, Iona I; Cochran, Barbara B; Croteau-Chonka, Damien C DC; Dumitrescu, Logan L; Eaton, Charles B CB; Franceschini, Nora N; Guo, Xiuqing X; Henderson, Brian E BE; Hindorff, Lucia A LA; Kim, Eric E; Kinnunen, Leena L; Komulainen, Pirjo P; Lee, Wen-Jane WJ; Le Marchand, Loic L; Lin, Yi Y; Lindström, Jaana J; Lingaas-Holmen, Oddgeir O; Mitchell, Sabrina L SL; Narisu, Narisu N; Robinson, Jennifer G JG; Schumacher, Fred F; Stančáková, Alena A; Sundvall, Jouko J; Sung, Yun-Ju YJ; Swift, Amy J AJ; Wang, Wen-Chang WC; Wilkens, Lynne L; Wilsgaard, Tom T; Young, Alicia M AM; Adair, Linda S LS; Ballantyne, Christie M CM; Bůžková, Petra P; Chakravarti, Aravinda A; Collins, Francis S FS; Duggan, David D; Feranil, Alan B AB; Ho, Low-Tone LT; Hung, Yi-Jen YJ; Hunt, Steven C SC; Hveem, Kristian K; Juang, Jyh-Ming J JM; Kesäniemi, Antero Y AY; Kuusisto, Johanna J; Laakso, Markku M; Lakka, Timo A TA; Lee, I-Te IT; Leppert, Mark F MF; Matise, Tara C TC; Moilanen, Leena L; Njølstad, Inger I; Peters, Ulrike U; Quertermous, Thomas T; Rauramaa, Rainer R; Rotter, Jerome I JI; Saramies, Jouko J; Tuomilehto, Jaakko J; Uusitupa, Matti M; Wang, Tzung-Dau TD; Boehnke, Michael M; Haiman, Christopher A CA; Chen, Yii-Der I YD; Kooperberg, Charles C; Assimes, Themistocles L TL; Crawford, Dana C DC; Hsiung, Chao A CA; North, Kari E KE; Mohlke, Karen L KL
Publication Date: 2013-03

Variant appearance in text: APOE: R163C; rs769455
PubMed Link: 23555291
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic factors for choroidal neovascularization associated with high myopia.

Investigative Ophthalmology & Visual Science
Leveziel, Nicolas N; Yu, Yi Y; Reynolds, Robyn R; Tai, Albert A; Meng, Weihua W; Caillaux, Violaine V; Calvas, Patrick P; Rosner, Bernard B; Malecaze, François F; Souied, Eric H EH; Seddon, Johanna M JM
Publication Date: 2012-07-27

Variant appearance in text: rs769455
PubMed Link: 22678500
Variant Present in the following documents:
  • Main text
View BVdb publication page



Screening and Evaluation of Deleterious SNPs in APOE Gene of Alzheimer's Disease.

Neurology Research International
Masoodi, Tariq Ahmad TA; Al Shammari, Sulaiman A SA; Al-Muammar, May N MN; Alhamdan, Adel A AA
Publication Date: 2012

Variant appearance in text: APOE: R163C; rs769455
PubMed Link: 22530123
Variant Present in the following documents:
  • Main text
View BVdb publication page



The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Rizzi, Thais S TS; Arias-Vasquez, Alejandro A; Rommelse, Nanda N; Kuntsi, Jonna J; Anney, Richard R; Asherson, Philip P; Buitelaar, Jan J; Banaschewski, Tobias T; Ebstein, Richard R; Ruano, Dina D; Van der Sluis, Sophie S; Markunas, Christina A CA; Garrett, Melanie E ME; Ashley-Koch, Allison E AE; Kollins, Scott H SH; Anastopoulos, Arthur D AD; Hansell, Narelle K NK; Wright, Margaret J MJ; Montgomery, Grant W GW; Martin, Nicholas G NG; Harris, Sarah E SE; Davies, Gail G; Tenesa, Albert A; Porteous, David J DJ; Starr, John M JM; Deary, Ian J IJ; St Pourcain, Beate B; Davey Smith, George G; Timpson, Nicholas J NJ; Evans, David M DM; Gill, Michael M; Miranda, Ana A; Mulas, Fernando F; Oades, Robert D RD; Roeyers, Herbert H; Rothenberger, Aribert A; Sergeant, Joseph J; Sonuga-Barke, Edmund E; Steinhausen, Hans Christoph HC; Taylor, Eric E; Faraone, Stephen V SV; Franke, Barbara B; Posthuma, Danielle D
Publication Date: 2011-03

Variant appearance in text: rs769455
PubMed Link: 21302343
Variant Present in the following documents:
  • Main text
View BVdb publication page



Subarachnoid hemorrhage: tests of association with apolipoprotein E and elastin genes.

Bmc Medical Genetics
Kaushal, Ritesh R; Woo, Daniel D; Pal, Prodipto P; Haverbusch, Mary M; Xi, Huifeng H; Moomaw, Charles C; Sekar, Padmini P; Kissela, Brett B; Kleindorfer, Dawn D; Flaherty, Matthew M; Sauerbeck, Laura L; Chakraborty, Ranajit R; Broderick, Joseph J; Deka, Ranjan R
Publication Date: 2007-07-31

Variant appearance in text: rs769455
PubMed Link: 17672902
Variant Present in the following documents:
  • Main text
View BVdb publication page