NINJ2 c.34-41794C>T

Variant ID: 12-717138-G-A

NM_016533.6(NINJ2):c.34-41794C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


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: rs2075032
PubMed Link: 24022295
Variant Present in the following documents:
  • Main text
View BVdb publication page