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