SIRT1 c.1915+1559A>C

Variant ID: 10-69674347-A-C

NM_012238.4(SIRT1):c.1915+1559A>C

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:

Sparse whole-genome sequencing identifies two loci for major depressive disorder.

Nature
,
Publication Date: 2015-07-30

Variant appearance in text: rs16924945
PubMed Link: 26176920
Variant Present in the following documents:
  • Main text
  • emss-63824.pdf
View BVdb publication page