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rs75493593

From SNPedia

Orientationplus
Stabilizedplus
Make rs75493593(G;G)
Make rs75493593(G;T)
Make rs75493593(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position7041768
GeneSLC16A11
is asnp
is mentioned by
dbSNPrs75493593
dbSNP (classic)rs75493593
ClinGenrs75493593
ebirs75493593
HLIrs75493593
Exacrs75493593
Gnomadrs75493593
Varsomers75493593
LitVarrs75493593
Maprs75493593
PheGenIrs75493593
Biobankrs75493593
1000 genomesrs75493593
hgdprs75493593
ensemblrs75493593
geneviewrs75493593
scholarrs75493593
googlers75493593
pharmgkbrs75493593
gwascentralrs75493593
openSNPrs75493593
23andMers75493593
SNPshotrs75493593
SNPdbers75493593
MSV3drs75493593
GWAS Ctlgrs75493593
Max Magnitude0
GWAS snp
PMID [PMID 24390345OA-icon.png]
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 30696834OA-icon.png] Associations between SLC16A11 variants and diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL).