rs2334499
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2334499(C;C) |
Make rs2334499(C;T) |
Make rs2334499(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 1675619 |
is a | snp |
is | mentioned by |
dbSNP | rs2334499 |
dbSNP (classic) | rs2334499 |
ClinGen | rs2334499 |
ebi | rs2334499 |
HLI | rs2334499 |
Exac | rs2334499 |
Gnomad | rs2334499 |
Varsome | rs2334499 |
LitVar | rs2334499 |
Map | rs2334499 |
PheGenI | rs2334499 |
Biobank | rs2334499 |
1000 genomes | rs2334499 |
hgdp | rs2334499 |
ensembl | rs2334499 |
geneview | rs2334499 |
scholar | rs2334499 |
rs2334499 | |
pharmgkb | rs2334499 |
gwascentral | rs2334499 |
openSNP | rs2334499 |
23andMe | rs2334499 |
SNPshot | rs2334499 |
SNPdbe | rs2334499 |
MSV3d | rs2334499 |
GWAS Ctlg | rs2334499 |
GMAF | 0.4532 |
Max Magnitude | 0 |
? | (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 20016592]
[PMID 21278902] Genetic risk profiling for prediction of type 2 diabetes.
[PMID 23462794] Identification of CpG-SNPs associated with type 2 diabetes and differential DNA methylation in human pancreatic islets.
[PMID 23630301] Strong parent-of-origin effects in the association of KCNQ1 variants with type 2 diabetes in American Indians.