CELF6 c.4G>A ;(p.A2T)

Variant ID: 15-72612212-C-T

NM_052840.4(CELF6):c.4G>A;(p.A2T)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

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: rs17855555
PubMed Link: 18485661
Variant Present in the following documents:
  • Main text
View BVdb publication page