Bibliome.ai browser hg19
Search
About
Stats
FAQ
CDH1 c.163+1854C>T
Variant ID: 16-68774168-C-T
NM_004360.3(
CDH1
):c.163+1854C>T
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Evaluating genetic variants associated with breast cancer risk in high and moderate-penetrance genes in Asians.
Carcinogenesis
Han, Mi-Ryung MR; Zheng, Wei W; Cai, Qiuyin Q; Gao, Yu-Tang YT; Zheng, Ying Y; Bolla, Manjeet K MK; Michailidou, Kyriaki K; Dennis, Joe J; Wang, Qin Q; Dunning, Alison M AM; Brennan, Paul P; Chen, Shou-Tung ST; Choi, Ji-Yeob JY; Hartman, Mikael M; Ito, Hidemi H; Lophatananon, Artitaya A; Matsuo, Keitaro K; Miao, Hui H; Muir, Kenneth K; Sangrajrang, Suleeporn S; Shen, Chen-Yang CY; Teo, Soo Hwang SH; Tseng, Chiu-Chen CC; Wu, Anna H AH; Yip, Cheng Har CH; Kang, Daehee D; Xiang, Yong-Bing YB; Easton, Douglas F DF; Shu, Xiao-Ou XO; Long, Jirong J
Publication Date: 2017-05-01
Variant appearance in text: rs2902185
PubMed Link:
28419251
Variant Present in the following documents:
Main text
View BVdb publication page