HCAR2 c.526T>A ;(p.L176M)

Variant ID: 12-123187305-A-T

NM_177551.3(HCAR2):c.526T>A;(p.L176M)

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:

The association of common SNPs and haplotypes in CETP gene with HDL cholesterol levels in Latvian population.

Plos One
Radovica, Ilze I; Fridmanis, Davids D; Vaivade, Iveta I; Nikitina-Zake, Liene L; Klovins, Janis J
Publication Date: 2013

Variant appearance in text: rs676404
PubMed Link: 23675527
Variant Present in the following documents:
  • Main text
  • pone.0064191.pdf
View BVdb publication page