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rs2334499

From SNPedia

Orientationplus
Stabilizedplus
Make rs2334499(C;C)
Make rs2334499(C;T)
Make rs2334499(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position1675619
is asnp
is mentioned by
dbSNPrs2334499
ebirs2334499
HLIrs2334499
Exacrs2334499
Varsomers2334499
Maprs2334499
PheGenIrs2334499
hapmaprs2334499
1000 genomesrs2334499
hgdprs2334499
ensemblrs2334499
gopubmedrs2334499
geneviewrs2334499
scholarrs2334499
googlers2334499
pharmgkbrs2334499
gwascentralrs2334499
openSNPrs2334499
23andMers2334499
23andMe allrs2334499
SNP Nexus

SNPshotrs2334499
SNPdbers2334499
MSV3drs2334499
GWAS Ctlgrs2334499
GMAF0.4532
Max Magnitude
? (C;C) (C;T) (T;T) 28
rs2334499 is in a region of chromosome 11p15 which contains a cluster of imprinted genes.

This SNP, rs2334499, has recently been reported to have an association with type-2 diabetes. The allele that confers risk when paternally inherited is protective when maternally inherited.[PMID 20016592OA-icon.png]

OMIM125853
Desc
Variant
Relatedalso
[PMID 21278902OA-icon.png] Genetic risk profiling for prediction of type 2 diabetes.


[PMID 23462794OA-icon.png] Identification of CpG-SNPs associated with type 2 diabetes and differential DNA methylation in human pancreatic islets.


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