AGO2 c.337-3987C>G

Variant ID: 8-141576720-G-C

NM_012154.3(AGO2):c.337-3987C>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:

A genome-wide association study of tinnitus reveals shared genetic links to neuropsychiatric disorders.

Scientific Reports
Bhatt, Ishan Sunilkumar IS; Wilson, Nicholas N; Dias, Raquel R; Torkamani, Ali A
Publication Date: 2022-12-29

Variant appearance in text: rs2977458
PubMed Link: 36581688
Variant Present in the following documents:
  • Main text
  • 41598_2022_Article_26413.pdf
View BVdb publication page