rs75493593
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs75493593(G;G) |
Make rs75493593(G;T) |
Make rs75493593(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 7041768 |
Gene | SLC16A11 |
is a | snp |
is | mentioned by |
dbSNP | rs75493593 |
dbSNP (classic) | rs75493593 |
ClinGen | rs75493593 |
ebi | rs75493593 |
HLI | rs75493593 |
Exac | rs75493593 |
Gnomad | rs75493593 |
Varsome | rs75493593 |
LitVar | rs75493593 |
Map | rs75493593 |
PheGenI | rs75493593 |
Biobank | rs75493593 |
1000 genomes | rs75493593 |
hgdp | rs75493593 |
ensembl | rs75493593 |
geneview | rs75493593 |
scholar | rs75493593 |
rs75493593 | |
pharmgkb | rs75493593 |
gwascentral | rs75493593 |
openSNP | rs75493593 |
23andMe | rs75493593 |
SNPshot | rs75493593 |
SNPdbe | rs75493593 |
MSV3d | rs75493593 |
GWAS Ctlg | rs75493593 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 24390345] |
Trait | Type 2 diabetes |
Title | Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico. |
Risk Allele | |
P-val | 5E-15 |
Odds Ratio | 1.25 [1.18-1.32] |
[PMID 30696834] Associations between SLC16A11 variants and diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL).