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FHIT c.-111+32119C>A
Variant ID: 3-60995600-G-T
NM_002012.4(
FHIT
):c.-111+32119C>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 association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population.
Scientific Reports
Zhou, Sirui S; Gan-Or, Ziv Z; Ambalavanan, Amirthagowri A; Lai, Dongbing D; Xie, Pingxing P; Bourassa, Cynthia V CV; Strong, Stephanie S; Ross, Jay P JP; Dionne-Laporte, Alexandre A; Spiegelman, Dan D; Dupré, Nicolas N; Foroud, Tatiana M TM; Xiong, Lan L; Dion, Patrick A PA; Rouleau, Guy A GA
Publication Date: 2018-03-12
Variant appearance in text: rs6782531
PubMed Link:
29531279
Variant Present in the following documents:
Main text
41598_2018_Article_21603.pdf
View BVdb publication page