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.




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