rs10911021
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10911021(C;C) |
Make rs10911021(C;T) |
Make rs10911021(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 182112825 |
Gene | LOC105371642, ZNF648 |
is a | snp |
is | mentioned by |
dbSNP | rs10911021 |
dbSNP (classic) | rs10911021 |
ClinGen | rs10911021 |
ebi | rs10911021 |
HLI | rs10911021 |
Exac | rs10911021 |
Gnomad | rs10911021 |
Varsome | rs10911021 |
LitVar | rs10911021 |
Map | rs10911021 |
PheGenI | rs10911021 |
Biobank | rs10911021 |
1000 genomes | rs10911021 |
hgdp | rs10911021 |
ensembl | rs10911021 |
geneview | rs10911021 |
scholar | rs10911021 |
rs10911021 | |
pharmgkb | rs10911021 |
gwascentral | rs10911021 |
openSNP | rs10911021 |
23andMe | rs10911021 |
SNPshot | rs10911021 |
SNPdbe | rs10911021 |
MSV3d | rs10911021 |
GWAS Ctlg | rs10911021 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23982368] |
Trait | Cardiovascular heart disease in diabetics |
Title | Association between a genetic variant related to glutamic acid metabolism and coronary heart disease in individuals with type 2 diabetes. |
Risk Allele | C |
P-val | 2E-8 |
Odds Ratio | 1.36 [1.22-1.51] |
[PMID 25677913] Genetic variant at the GLUL locus predicts all-cause mortality in patients with type 2 diabetes
[PMID 27549350] Variant rs10911021 that associates with coronary heart disease in type 2 diabetes, is associated with lower concentrations of circulating HDL cholesterol and large HDL particles but not with amino acids.
[PMID 29304826] The SNP rs10911021 is associated with oxidative stress in coronary heart disease patients from Pakistan.