EFEMP2 c.934A>G ;(p.T312A)

Variant ID: 11-65635806-T-C

NM_016938.4(EFEMP2):c.934A>G;(p.T312A)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Rare coding variants and breast cancer risk: evaluation of susceptibility Loci identified in genome-wide association studies.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Zhang, Yanfeng Y; Long, Jirong J; Lu, Wei W; Shu, Xiao-Ou XO; Cai, Qiuyin Q; Zheng, Ying Y; Li, Chun C; Li, Bingshan B; Gao, Yu-Tang YT; Zheng, Wei W
Publication Date: 2014-04

Variant appearance in text: EFEMP2: Thr312Ala
PubMed Link: 24470074
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide testing of putative functional exonic variants in relationship with breast and prostate cancer risk in a multiethnic population.

Plos Genetics
Haiman, Christopher A CA; Han, Ying Y; Feng, Ye Y; Xia, Lucy L; Hsu, Chris C; Sheng, Xin X; Pooler, Loreall C LC; Patel, Yesha Y; Kolonel, Laurence N LN; Carter, Erin E; Park, Karen K; Le Marchand, Loic L; Van Den Berg, David D; Henderson, Brian E BE; Stram, Daniel O DO
Publication Date: 2013-03

Variant appearance in text: rs148410446
PubMed Link: 23555315
Variant Present in the following documents:
  • pgen.1003419.s008.xlsx, sheet 1
View BVdb publication page