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FHIT c.348+27688A>G
Variant ID: 3-59880384-T-C
NM_002012.2(
FHIT
):c.348+27688A>G
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: rs750793
PubMed Link:
18485661
Variant Present in the following documents:
Main text
View BVdb publication page