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