PCSK7 c.1054+381A>G

Variant ID: 11-117094413-T-C

NM_004716.2(PCSK7):c.1054+381A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Multiple phenotype association tests using summary statistics in genome-wide association studies.

Biometrics
Liu, Zhonghua Z; Lin, Xihong X
Publication Date: 2018-03

Variant appearance in text: rs11216321
PubMed Link: 28653391
Variant Present in the following documents:
  • Main text
View BVdb publication page