Bibliome.ai browser hg19
Search
About
Stats
FAQ
DNAJA4 c.877+1860A>G
Variant ID: 15-78569930-A-G
NM_001130182.1(
DNAJA4
):c.877+1860A>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 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: rs8032417
PubMed Link:
29531279
Variant Present in the following documents:
Main text
41598_2018_21603_MOESM1_ESM.pdf
41598_2018_Article_21603.pdf
View BVdb publication page