CELF6 c.1406T>C ;(p.V469A)

Variant ID: 15-72579646-A-G

NM_052840.4(CELF6):c.1406T>C;(p.V469A)

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: rs17852852
PubMed Link: 18485661
Variant Present in the following documents:
  • Main text
View BVdb publication page