SORCS3 c.796-28796C>A

Variant ID: 10-106708297-C-A

NM_014978.1(SORCS3):c.796-28796C>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:

Pharmacogenetic effects of 'candidate gene complexes' on stroke in the GenHAT study.

Pharmacogenetics And Genomics
Sørensen, Izel F IF; Vazquez, Ana I AI; Irvin, Marguerite R MR; Sørensen, Peter P; Davis, Barry R BR; Ford, Charles E CE; Boerwinkle, Eric E; Eckfeldt, John H JH; Arnett, Donna K DK
Publication Date: 2014-11

Variant appearance in text: rs4917434
PubMed Link: 25171760
Variant Present in the following documents:
  • Main text
View BVdb publication page