GRM5 c.912-49638T>A

Variant ID: 11-88436209-A-T

NM_001143831.2(GRM5):c.912-49638T>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genome-wide SNP typing reveals signatures of population history.

Genomics
Hughes, Austin L AL; Welch, Robert R; Puri, Vinita V; Matthews, Casey C; Haque, Kashif K; Chanock, Stephen J SJ; Yeager, Meredith M
Publication Date: 2008-07

Variant appearance in text: rs10741500
PubMed Link: 18485661
Variant Present in the following documents:
  • Main text
View BVdb publication page