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rs10911021

From SNPedia

Orientationplus
Stabilizedplus
Make rs10911021(C;C)
Make rs10911021(C;T)
Make rs10911021(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position182112825
is asnp
is mentioned by
dbSNPrs10911021
ebirs10911021
HLIrs10911021
Exacrs10911021
Varsomers10911021
Maprs10911021
PheGenIrs10911021
hapmaprs10911021
1000 genomesrs10911021
hgdprs10911021
ensemblrs10911021
gopubmedrs10911021
geneviewrs10911021
scholarrs10911021
googlers10911021
pharmgkbrs10911021
gwascentralrs10911021
openSNPrs10911021
23andMers10911021
23andMe allrs10911021
SNP Nexus

SNPshotrs10911021
SNPdbers10911021
MSV3drs10911021
GWAS Ctlgrs10911021
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23982368OA-icon.png]
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.