ARHGAP10 c.154+43311T>C

Variant ID: 4-148696917-T-C

NM_024605.3(ARHGAP10):c.154+43311T>C

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: rs11729081
PubMed Link: 18485661
Variant Present in the following documents:
  • Main text
View BVdb publication page