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SYN3 c.369+12631C>A
Variant ID: 22-33363999-G-T
NM_003490.3(
SYN3
):c.369+12631C>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 study of 14,000 cases of seven common diseases and 3,000 shared controls.
Nature
,
Publication Date: 2007-06-07
Variant appearance in text: rs11089599
PubMed Link:
17554300
Variant Present in the following documents:
Main text
View BVdb publication page