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rs231362

From SNPedia

Orientationminus
Stabilizedminus
Make rs231362(C;C)
Make rs231362(C;T)
Make rs231362(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2670241
GeneKCNQ1, KCNQ1OT1
is asnp
is mentioned by
dbSNPrs231362
ClinGenrs231362
ebirs231362
HLIrs231362
Exacrs231362
Varsomers231362
Maprs231362
PheGenIrs231362
hapmaprs231362
1000 genomesrs231362
hgdprs231362
ensemblrs231362
gopubmedrs231362
geneviewrs231362
scholarrs231362
googlers231362
pharmgkbrs231362
gwascentralrs231362
openSNPrs231362
23andMers231362
23andMe allrs231362
SNP Nexus

SNPshotrs231362
SNPdbers231362
MSV3drs231362
GWAS Ctlgrs231362
GMAF0.3191
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20581827OA-icon.png]
Trait Type 2 diabetes
Title Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
Risk Allele G
P-val 3E-13
Odds Ratio 1.08 [1.06-1.10]
OMIM125853
Desc
Variant
Relatedalso
[PMID 21261977OA-icon.png] Variants in KCNQ1 increase type II diabetes susceptibility in South Asians: a study of 3,310 subjects from India and the US.


[PMID 21278902OA-icon.png] Genetic risk profiling for prediction of type 2 diabetes.


[PMID 23271129] Meta-analysis of the effect of KCNQ1 gene polymorphism on the risk of type 2 diabetes


[PMID 23043714] Genome-wide association studies-derived susceptibility loci in type 2 diabetes: confirmation in a Chinese population.


[PMID 23532257OA-icon.png] Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4.


[PMID 23630301OA-icon.png] Strong parent-of-origin effects in the association of KCNQ1 variants with type 2 diabetes in American Indians.