HERC2 c.3685G>A ;(p.D1229N)

Variant ID: 15-28483811-C-T

NM_004667.5(HERC2):c.3685G>A;(p.D1229N)

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: HERC2: Asp1229Asn
PubMed Link: 20876667
Variant Present in the following documents:
  • Main text
View BVdb publication page