BRCA1 c.4357+117G>A

Variant ID: 17-41234304-C-T

NM_007294.3(BRCA1):c.4357+117G>A

This variant was identified in 29 publications

View GRCh38 version.




Publications:


Ethnic-specificity, evolution origin and deleteriousness of Asian BRCA variation revealed by over 7500 BRCA variants derived from Asian population.

International Journal Of Cancer
Qin, Zixin Z; Li, Jiaheng J; Tam, Benjamin B; Sinha, Siddharth S; Zhao, Bojin B; Bhaskaran, Shanmuga Priya SP; Huang, Teng T; Wu, Xiaobing X; Chian, Jia Sheng JS; Guo, Maoni M; Kou, Si Hoi SH; Lei, Huijun H; Zhang, Li L; Wang, Xiaoyu X; Lagniton, Philip Naderev P PNP; Xiao, Fengxia F; Jiang, Xinyang X; Wang, San Ming SM
Publication Date: 2022-11-17

Variant appearance in text: BRCA1: 4357+117G>A; rs3737559
PubMed Link: 36385461
Variant Present in the following documents:
  • IJC-152-1159-s002.xlsx, sheet 1
  • IJC-152-1159-s006.xlsx, sheet 2
  • IJC-152-1159-s009.xlsx, sheet 2
View BVdb publication page



Mutational landscape and genetic signatures of cell-free DNA in tumour-induced osteomalacia.

Journal Of Cellular And Molecular Medicine
Wu, Nan N; Zhang, Zhen Z; Zhou, Xi X; Zhao, Hengqiang H; Ming, Yue Y; Wu, Xue X; Zhang, Xian X; Yang, Xin-Zhuang XZ; Zhou, Meng M; Bao, Hua H; Chen, Weisheng W; Wu, Yong Y; Liu, Sen S; Wang, Huizi H; Niu, Yuchen Y; Li, Yalun Y; Zheng, Yu Y; Shao, Yang Y; Gao, Na N; Yang, Ying Y; Liu, Ying Y; Li, Wenli W; Liu, Jia J; Zhang, Na N; Yang, Xu X; Xu, Yuan Y; Li, Mei M; Sun, Yingli Y; Su, Jianzhong J; Zhang, Jianguo J; Xia, Weibo W; Qiu, Guixing G; Liu, Yong Y; Liu, Jiaqi J; Wu, Zhihong Z
Publication Date: 2020-05

Variant appearance in text: BRCA1: 4357+117G>A
PubMed Link: 32277576
Variant Present in the following documents:
  • JCMM-24-4931-s010.xlsx, sheet 1
View BVdb publication page



PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology
Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S
Publication Date: 2019-10-22

Variant appearance in text: BRCA1: 4357+117G>A; rs3737559
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Correlation between Candidate Single Nucleotide Variants and Several Clinicopathological Risk Factors Related to Breast Cancer in Jordanian Women: A Genotype-Phenotype Study.

Journal Of Cancer
Al-Eitan, Laith N LN; Rababa'h, Doaa M DM; Alghamdi, Mansour A MA; Khasawneh, Rame H RH
Publication Date: 2019

Variant appearance in text: rs3737559
PubMed Link: 31528229
Variant Present in the following documents:
  • Main text
  • jcav10p4647.pdf
View BVdb publication page



Germline variation in BRCA1/2 is highly ethnic-specific: Evidence from over 30,000 Chinese hereditary breast and ovarian cancer patients.

International Journal Of Cancer
Bhaskaran, Shanmuga Priya SP; Chandratre, Khyati K; Gupta, Hemant H; Zhang, Li L; Wang, Xiaoyu X; Cui, Jian J; Kim, Yeong C YC; Sinha, Siddharth S; Jiang, Luhan L; Lu, Boya B; Wu, Xiaobing X; Qin, Zixin Z; Huang, Teng T; Wang, San Ming SM
Publication Date: 2019-08-15

Variant appearance in text: rs3737559
PubMed Link: 30702160
Variant Present in the following documents:
  • IJC-145-962-s004.xlsx, sheet 1
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs3737559
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



A Chinese family affected by lynch syndrome caused by MLH1 mutation.

Bmc Medical Genetics
Jia, Shuqin S; Zhang, Meng M; Sun, Yu Y; Yan, Hai H; Zhao, Fangping F; Li, Ziyu Z; Ji, Jiafu J
Publication Date: 2018-06-22

Variant appearance in text: rs3737559
PubMed Link: 29929473
Variant Present in the following documents:
  • 12881_2018_605_MOESM2_ESM.xlsx, sheet 1
  • 12881_2018_605_MOESM2_ESM.xlsx, sheet 2
View BVdb publication page



Sources of discordance among germ-line variant classifications in ClinVar.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Yang, Shan S; Lincoln, Stephen E SE; Kobayashi, Yuya Y; Nykamp, Keith K; Nussbaum, Robert L RL; Topper, Scott S
Publication Date: 2017-10

Variant appearance in text: BRCA1: 4357+117G>A
PubMed Link: 28569743
Variant Present in the following documents:
  • gim201760x7.xlsx, sheet 2
View BVdb publication page



Relevance of DNA repair gene polymorphisms to gastric cancer risk and phenotype.

Oncotarget
Carrera-Lasfuentes, Patricia P; Lanas, Angel A; Bujanda, Luis L; Strunk, Mark M; Quintero, Enrique E; Santolaria, Santos S; Benito, Rafael R; Sopeña, Federico F; Piazuelo, Elena E; Thomson, Concha C; Pérez-Aisa, Angeles A; Nicolás-Pérez, David D; Hijona, Elizabeth E; Espinel, Jesús J; Campo, Rafael R; Manzano, Marisa M; Geijo, Fernando F; Pellise, María M; Zaballa, Manuel M; González-Huix, Ferrán F; Espinós, Jorge J; Titó, Llúcia L; Barranco, Luis L; D'Amato, Mauro M; García-González, María Asunción MA
Publication Date: 2017-05-30

Variant appearance in text: rs3737559
PubMed Link: 28415781
Variant Present in the following documents:
  • Main text
View BVdb publication page



Unique Features of Germline Variation in Five Egyptian Familial Breast Cancer Families Revealed by Exome Sequencing.

Plos One
Kim, Yeong C YC; Soliman, Amr S AS; Cui, Jian J; Ramadan, Mohamed M; Hablas, Ahmed A; Abouelhoda, Mohamed M; Hussien, Nehal N; Ahmed, Ola O; Zekri, Abdel-Rahman Nabawy AN; Seifeldin, Ibrahim A IA; Wang, San Ming SM
Publication Date: 2017

Variant appearance in text: BRCA1: 4357+117G>A; rs3737559
PubMed Link: 28076423
Variant Present in the following documents:
  • Main text
View BVdb publication page



Novel BRCA1 and BRCA2 Tumor Test as Basis for Treatment Decisions and Referral for Genetic Counselling of Patients with Ovarian Carcinomas.

Human Mutation
Weren, Robbert D A RD; Mensenkamp, Arjen R AR; Simons, Michiel M; Eijkelenboom, Astrid A; Sie, Aisha S AS; Ouchene, Hicham H; van Asseldonk, Monique M; Gomez-Garcia, Encarna B EB; Blok, Marinus J MJ; de Hullu, Joanne A JA; Nelen, Marcel R MR; Hoischen, Alexander A; Bulten, Johan J; Tops, Bastiaan B J BB; Hoogerbrugge, Nicoline N; Ligtenberg, Marjolijn J L MJ
Publication Date: 2017-02

Variant appearance in text: BRCA1: 4357+117G>A
PubMed Link: 27767231
Variant Present in the following documents:
  • HUMU-38-226-s002.xlsx, sheet 3
View BVdb publication page



Common variation in BRCA1 may have a role in progression to lethal prostate cancer after radiation treatment.

Prostate Cancer And Prostatic Diseases
Sanchez, A A; Schoenfeld, J D JD; Nguyen, P L PL; Fiorentino, M M; Chowdhury, D D; Stampfer, M J MJ; Sesso, H D HD; Giovannucci, E E; Mucci, L A LA; Shui, I M IM
Publication Date: 2016-06

Variant appearance in text: rs3737559
PubMed Link: 26926928
Variant Present in the following documents:
  • Main text
View BVdb publication page



Estimation of the RNU2 macrosatellite mutation rate by BRCA1 mutation tracing.

Nucleic Acids Research
Tessereau, Chloé C; Lesecque, Yann Y; Monnet, Nastasia N; Buisson, Monique M; Barjhoux, Laure L; Léoné, Mélanie M; Feng, Bingjian B; Goldgar, David E DE; Sinilnikova, Olga M OM; Mousset, Sylvain S; Duret, Laurent L; Mazoyer, Sylvie S
Publication Date: 2014-08

Variant appearance in text: rs3737559
PubMed Link: 25034697
Variant Present in the following documents:
  • supp_gku639_nar-00908-d-2014-File008.xlsx, sheet 1
View BVdb publication page



Genetic variation of the brca1 and brca2 genes in macedonian patients.

Balkan Journal Of Medical Genetics : Bjmg
Maleva, I I; Madjunkova, S S; Bozhinovski, G G; Smickova, E E; Kondov, G G; Spiroski, Z Z; Arsovski, A A; Plaseska-Karanfilska, D D
Publication Date: 2012-12

Variant appearance in text: rs3737559
PubMed Link: 24052750
Variant Present in the following documents:
  • Main text
  • bjmg-15-02a-81.pdf
View BVdb publication page



Lung cancer and DNA repair genes: multilevel association analysis from the International Lung Cancer Consortium.

Carcinogenesis
Kazma, Rémi R; Babron, Marie-Claude MC; Gaborieau, Valérie V; Génin, Emmanuelle E; Brennan, Paul P; Hung, Rayjean J RJ; McLaughlin, John R JR; Krokan, Hans E HE; Elvestad, Maiken B MB; Skorpen, Frank F; Anderssen, Endre E; Vooder, Tõnu T; Välk, Kristjan K; Metspalu, Andres A; Field, John K JK; Lathrop, Mark M; Sarasin, Alain A; Benhamou, Simone S; ,
Publication Date: 2012-05

Variant appearance in text: rs3737559
PubMed Link: 22382497
Variant Present in the following documents:
  • Main text
View BVdb publication page



Folate and vitamin B12-related genes and risk for omphalocele.

Human Genetics
Mills, James L JL; Carter, Tonia C TC; Kay, Denise M DM; Browne, Marilyn L ML; Brody, Lawrence C LC; Liu, Aiyi A; Romitti, Paul A PA; Caggana, Michele M; Druschel, Charlotte M CM
Publication Date: 2012-05

Variant appearance in text: rs3737559
PubMed Link: 22116453
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association between single nucleotide polymorphisms on chromosome 17q and the risk of prostate cancer in a Chinese population.

Chinese Journal Of Cancer
Zhou, Chang-Hu CH; Wang, Jian-Ye JY; Cao, Su-Yan SY; Shi, Xiao-Hong XH; Zhang, Yao-Guang YG; Liu, Ming M; Wang, Xin X; Huang, Jin J; Yang, Yi-Ge YG; Wei, Dong D; Yang, Ze Z
Publication Date: 2011-10

Variant appearance in text: rs3737559
PubMed Link: 21959049
Variant Present in the following documents:
  • Main text
  • cjc-30-10-721.pdf
View BVdb publication page



Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers.

Human Molecular Genetics
Cox, David G DG; Simard, Jacques J; Sinnett, Daniel D; Hamdi, Yosr Y; Soucy, Penny P; Ouimet, Manon M; Barjhoux, Laure L; Verny-Pierre, Carole C; McGuffog, Lesley L; Healey, Sue S; Szabo, Csilla C; Greene, Mark H MH; Mai, Phuong L PL; Andrulis, Irene L IL; , ; Thomassen, Mads M; Gerdes, Anne-Marie AM; Caligo, Maria A MA; Friedman, Eitan E; Laitman, Yael Y; Kaufman, Bella B; Paluch, Shani S SS; Borg, Åke Å; Karlsson, Per P; Askmalm, Marie Stenmark MS; Bustinza, Gisela Barbany GB; , ; Nathanson, Katherine L KL; Domchek, Susan M SM; Rebbeck, Timothy R TR; Benítez, Javier J; Hamann, Ute U; Rookus, Matti A MA; van den Ouweland, Ans M W AM; Ausems, Margreet G E M MG; Aalfs, Cora M CM; van Asperen, Christi J CJ; Devilee, Peter P; Gille, Hans J J P HJ; , ; , ; Peock, Susan S; Frost, Debra D; Evans, D Gareth DG; Eeles, Ros R; Izatt, Louise L; Adlard, Julian J; Paterson, Joan J; Eason, Jacqueline J; Godwin, Andrew K AK; Remon, Marie-Alice MA; Moncoutier, Virginie V; Gauthier-Villars, Marion M; Lasset, Christine C; Giraud, Sophie S; Hardouin, Agnès A; Berthet, Pascaline P; Sobol, Hagay H; Eisinger, François F; Bressac de Paillerets, Brigitte B; Caron, Olivier O; Delnatte, Capucine C; , ; Goldgar, David D; Miron, Alex A; Ozcelik, Hilmi H; Buys, Saundra S; Southey, Melissa C MC; Terry, Mary Beth MB; , ; Singer, Christian F CF; Dressler, Anne-Catharina AC; Tea, Muy-Kheng MK; Hansen, Thomas V O TV; Johannsson, Oskar O; Piedmonte, Marion M; Rodriguez, Gustavo C GC; Basil, Jack B JB; Blank, Stephanie S; Toland, Amanda E AE; Montagna, Marco M; Isaacs, Claudine C; Blanco, Ignacio I; Gayther, Simon A SA; Moysich, Kirsten B KB; Schmutzler, Rita K RK; Wappenschmidt, Barbara B; Engel, Christoph C; Meindl, Alfons A; Ditsch, Nina N; Arnold, Norbert N; Niederacher, Dieter D; Sutter, Christian C; Gadzicki, Dorothea D; Fiebig, Britta B; Caldes, Trinidad T; Laframboise, Rachel R; Nevanlinna, Heli H; Chen, Xiaoqing X; Beesley, Jonathan J; Spurdle, Amanda B AB; Neuhausen, Susan L SL; Ding, Yuan C YC; Couch, Fergus J FJ; Wang, Xianshu X; Peterlongo, Paolo P; Manoukian, Siranoush S; Bernard, Loris L; Radice, Paolo P; Easton, Douglas F DF; Chenevix-Trench, Georgia G; Antoniou, Antonis C AC; Stoppa-Lyonnet, Dominique D; Mazoyer, Sylvie S; Sinilnikova, Olga M OM; ,
Publication Date: 2011-12-01

Variant appearance in text: rs3737559
PubMed Link: 21890493
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic predictors of taxane-induced neurotoxicity in a SWOG phase III intergroup adjuvant breast cancer treatment trial (S0221).

Breast Cancer Research And Treatment
Sucheston, Lara E LE; Zhao, Hua H; Yao, Song S; Zirpoli, Gary G; Liu, Song S; Barlow, William E WE; Moore, Halle C F HC; Thomas Budd, G G; Hershman, Dawn L DL; Davis, Warren W; Ciupak, Gregory L GL; Stewart, James A JA; Isaacs, Claudine C; Hobday, Timothy J TJ; Salim, Muhammad M; Hortobagyi, Gabriel N GN; Gralow, Julie R JR; Livingston, Robert B RB; Albain, Kathy S KS; Hayes, Daniel F DF; Ambrosone, Christine B CB
Publication Date: 2011-12

Variant appearance in text: rs3737559
PubMed Link: 21766209
Variant Present in the following documents:
  • Main text
View BVdb publication page



Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers.

Human Genetics
Im, Kate M KM; Kirchhoff, Tomas T; Wang, Xianshu X; Green, Todd T; Chow, Clement Y CY; Vijai, Joseph J; Korn, Joshua J; Gaudet, Mia M MM; Fredericksen, Zachary Z; Shane Pankratz, V V; Guiducci, Candace C; Crenshaw, Andrew A; McGuffog, Lesley L; Kartsonaki, Christiana C; Morrison, Jonathan J; Healey, Sue S; Sinilnikova, Olga M OM; Mai, Phuong L PL; Greene, Mark H MH; Piedmonte, Marion M; Rubinstein, Wendy S WS; , ; Hogervorst, Frans B FB; Rookus, Matti A MA; Collée, J Margriet JM; Hoogerbrugge, Nicoline N; van Asperen, Christi J CJ; Meijers-Heijboer, Hanne E J HE; Van Roozendaal, Cees E CE; Caldes, Trinidad T; Perez-Segura, Pedro P; Jakubowska, Anna A; Lubinski, Jan J; Huzarski, Tomasz T; Blecharz, Paweł P; Nevanlinna, Heli H; Aittomäki, Kristiina K; Lazaro, Conxi C; Blanco, Ignacio I; Barkardottir, Rosa B RB; Montagna, Marco M; D'Andrea, Emma E; , ; Devilee, Peter P; Olopade, Olufunmilayo I OI; Neuhausen, Susan L SL; Peissel, Bernard B; Bonanni, Bernardo B; Peterlongo, Paolo P; Singer, Christian F CF; Rennert, Gad G; Lejbkowicz, Flavio F; Andrulis, Irene L IL; Glendon, Gord G; Ozcelik, Hilmi H; , ; Toland, Amanda Ewart AE; Caligo, Maria Adelaide MA; , ; Beattie, Mary S MS; Chan, Salina S; , ; Domchek, Susan M SM; Nathanson, Katherine L KL; Rebbeck, Timothy R TR; Phelan, Catherine C; Narod, Steven S; John, Esther M EM; Hopper, John L JL; Buys, Saundra S SS; Daly, Mary B MB; Southey, Melissa C MC; Terry, Mary-Beth MB; Tung, Nadine N; Hansen, Thomas V O TV; Osorio, Ana A; Benitez, Javier J; Durán, Mercedes M; Weitzel, Jeffrey N JN; Garber, Judy J; Hamann, Ute U; , ; Peock, Susan S; Cook, Margaret M; Oliver, Clare T CT; Frost, Debra D; Platte, Radka R; Evans, D Gareth DG; Eeles, Ros R; Izatt, Louise L; Paterson, Joan J; Brewer, Carole C; Hodgson, Shirley S; Morrison, Patrick J PJ; Porteous, Mary M; Walker, Lisa L; Rogers, Mark T MT; Side, Lucy E LE; Godwin, Andrew K AK; Schmutzler, Rita K RK; Wappenschmidt, Barbara B; Laitman, Yael Y; Meindl, Alfons A; Deissler, Helmut H; Varon-Mateeva, Raymonda R; Preisler-Adams, Sabine S; Kast, Karin K; Venat-Bouvet, Laurence L; Stoppa-Lyonnet, Dominique D; Chenevix-Trench, Georgia G; Easton, Douglas F DF; Klein, Robert J RJ; Daly, Mark J MJ; Friedman, Eitan E; Dean, Michael M; Clark, Andrew G AG; Altshuler, David M DM; Antoniou, Antonis C AC; Couch, Fergus J FJ; Offit, Kenneth K; Gold, Bert B
Publication Date: 2011-11

Variant appearance in text: rs3737559
PubMed Link: 21597964
Variant Present in the following documents:
  • Main text
View BVdb publication page



Evaluation of 64 candidate single nucleotide polymorphisms as risk factors for neural tube defects in a large Irish study population.

American Journal Of Medical Genetics. Part A
Carter, Tonia C TC; Pangilinan, Faith F; Troendle, James F JF; Molloy, Anne M AM; VanderMeer, Julia J; Mitchell, Adam A; Kirke, Peadar N PN; Conley, Mary R MR; Shane, Barry B; Scott, John M JM; Brody, Lawrence C LC; Mills, James L JL
Publication Date: 2011-01

Variant appearance in text: rs3737559
PubMed Link: 21204206
Variant Present in the following documents:
  • Main text
View BVdb publication page



Risk of contralateral breast cancer associated with common variants in BRCA1 and BRCA2: potential modifying effect of BRCA1/BRCA2 mutation carrier status.

Breast Cancer Research And Treatment
Figueiredo, Jane C JC; Brooks, Jennifer D JD; Conti, David V DV; Poynter, Jenny N JN; Teraoka, Sharon N SN; Malone, Kathleen E KE; Bernstein, Leslie L; Lee, Won D WD; Duggan, David J DJ; Siniard, Ashley A; Concannon, Patrick P; Capanu, Marinela M; Lynch, Charles F CF; Olsen, Jørgen H JH; Haile, Robert W RW; Bernstein, Jonine L JL
Publication Date: 2011-06

Variant appearance in text: rs3737559
PubMed Link: 21161372
Variant Present in the following documents:
  • Main text
View BVdb publication page



Estimation of genotype relative risks from pedigree data by retrospective likelihoods.

Genetic Epidemiology
Schaid, Daniel J DJ; McDonnell, Shannon K SK; Riska, Shaun M SM; Carlson, Erin E EE; Thibodeau, Stephen N SN
Publication Date: 2010-05

Variant appearance in text: rs3737559
PubMed Link: 20039378
Variant Present in the following documents:
  • Main text
View BVdb publication page



Associations between single nucleotide polymorphisms in double-stranded DNA repair pathway genes and familial breast cancer.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Sehl, Mary E ME; Langer, Lucy R LR; Papp, Jeanette C JC; Kwan, Lorna L; Seldon, Joyce L JL; Arellano, Geovanni G; Reiss, Jean J; Reed, Elaine F EF; Dandekar, Sugandha S; Korin, Yael Y; Sinsheimer, Janet S JS; Zhang, Zuo-Feng ZF; Ganz, Patricia A PA
Publication Date: 2009-03-15

Variant appearance in text: rs3737559
PubMed Link: 19276285
Variant Present in the following documents:
  • Main text
View BVdb publication page



Chromosome 17q12 variants contribute to risk of early-onset prostate cancer.

Cancer Research
Levin, Albert M AM; Machiela, Mitchell J MJ; Zuhlke, Kimberly A KA; Ray, Anna M AM; Cooney, Kathleen A KA; Douglas, Julie A JA
Publication Date: 2008-08-15

Variant appearance in text: rs3737559
PubMed Link: 18701471
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common variation in the BRCA1 gene and prostate cancer risk.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Douglas, Julie A JA; Levin, Albert M AM; Zuhlke, Kimberly A KA; Ray, Anna M AM; Johnson, Gregory R GR; Lange, Ethan M EM; Wood, David P DP; Cooney, Kathleen A KA
Publication Date: 2007-07

Variant appearance in text: rs3737559
PubMed Link: 17585057
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common variants in the ATM, BRCA1, BRCA2, CHEK2 and TP53 cancer susceptibility genes are unlikely to increase breast cancer risk.

Breast Cancer Research : Bcr
Baynes, Caroline C; Healey, Catherine S CS; Pooley, Karen A KA; Scollen, Serena S; Luben, Robert N RN; Thompson, Deborah J DJ; Pharoah, Paul D P PD; Easton, Douglas F DF; Ponder, Bruce A J BA; Dunning, Alison M AM; ,
Publication Date: 2007

Variant appearance in text: rs3737559
PubMed Link: 17428325
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association between common variation in 120 candidate genes and breast cancer risk.

Plos Genetics
Pharoah, Paul D P PD; Tyrer, Jonathan J; Dunning, Alison M AM; Easton, Douglas F DF; Ponder, Bruce A J BA; ,
Publication Date: 2007-03-16

Variant appearance in text: rs3737559
PubMed Link: 17367212
Variant Present in the following documents:
View BVdb publication page



Haplotype analysis of common variants in the BRCA1 gene and risk of sporadic breast cancer.

Breast Cancer Research : Bcr
Cox, David G DG; Kraft, Peter P; Hankinson, Susan E SE; Hunter, David J DJ
Publication Date: 2005

Variant appearance in text: rs3737559
PubMed Link: 15743496
Variant Present in the following documents:
  • Main text
  • bcr973.pdf
View BVdb publication page