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NINJ2 c.34-21751G>C
Variant ID: 12-697095-C-G
NM_016533.6(
NINJ2
):c.34-21751G>C
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
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dbSNP
Publications:
iFunMed: Integrative functional mediation analysis of GWAS and eQTL studies.
Genetic Epidemiology
Rojo, Constanza C; Zhang, Qi Q; Keleş, Sündüz S
Publication Date: 2019-10
Variant appearance in text: rs11063749
PubMed Link:
31328826
Variant Present in the following documents:
Main text
View BVdb publication page
A fast multilocus test with adaptive SNP selection for large-scale genetic-association studies.
European Journal Of Human Genetics : Ejhg
Zhang, Han H; Shi, Jianxin J; Liang, Faming F; Wheeler, William W; Stolzenberg-Solomon, Rachael R; Yu, Kai K
Publication Date: 2014-05
Variant appearance in text: rs11063749
PubMed Link:
24022295
Variant Present in the following documents:
Main text
View BVdb publication page