BRCA2 c.8331+1616T>G

Variant ID: 13-32939286-T-G

NM_000059.3(BRCA2):c.8331+1616T>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: BRCA2: 8331+1616T>G; rs9534269
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Polymorphisms of the centrosomal gene (FGFR1OP) and lung cancer risk: a meta-analysis of 14,463 cases and 44,188 controls.

Carcinogenesis
Kang, Xiaozheng X; Liu, Hongliang H; Onaitis, Mark W MW; Liu, Zhensheng Z; Owzar, Kouros K; Han, Younghun Y; Su, Li L; Wei, Yongyue Y; Hung, Rayjean J RJ; Brhane, Yonathan Y; McLaughlin, John J; Brennan, Paul P; Bickeböller, Heike H; Rosenberger, Albert A; Houlston, Richard S RS; Caporaso, Neil N; Landi, Maria Teresa MT; Heinrich, Joachim J; Risch, Angela A; Wu, Xifeng X; Ye, Yuanqing Y; Christiani, David C DC; Amos, Christopher I CI; Wei, Qingyi Q; ,
Publication Date: 2016-03

Variant appearance in text: rs9534269
PubMed Link: 26905588
Variant Present in the following documents:
  • Main text
View BVdb publication page