OCA2 c.802C>T ;(p.Q268*)

Variant ID: 15-28263548-G-A

NM_000275.2(OCA2):c.802C>T;(p.Q268*)

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 significant associations for variants with minor allele frequency of 5% or less--an overview: A HuGE review.

American Journal Of Epidemiology
Panagiotou, Orestis A OA; Evangelou, Evangelos E; Ioannidis, John P A JP
Publication Date: 2010-10-15

Variant appearance in text: OCA2: Gln268Ter
PubMed Link: 20876667
Variant Present in the following documents:
  • Main text
View BVdb publication page