rs151290
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs151290(A;A) |
Make rs151290(A;C) |
Make rs151290(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 2800385 |
Gene | KCNQ1 |
is a | snp |
is | mentioned by |
dbSNP | rs151290 |
dbSNP (classic) | rs151290 |
ClinGen | rs151290 |
ebi | rs151290 |
HLI | rs151290 |
Exac | rs151290 |
Gnomad | rs151290 |
Varsome | rs151290 |
LitVar | rs151290 |
Map | rs151290 |
PheGenI | rs151290 |
Biobank | rs151290 |
1000 genomes | rs151290 |
hgdp | rs151290 |
ensembl | rs151290 |
geneview | rs151290 |
scholar | rs151290 |
rs151290 | |
pharmgkb | rs151290 |
gwascentral | rs151290 |
openSNP | rs151290 |
23andMe | rs151290 |
SNPshot | rs151290 |
SNPdbe | rs151290 |
MSV3d | rs151290 |
GWAS Ctlg | rs151290 |
GMAF | 0.3618 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 19366866] Association of type 2 diabetes candidate polymorphisms in KCNQ1 with incretin and insulin secretion
[PMID 20802253] Glycemia determines the effect of type 2 diabetes risk genes on insulin secretion
[PMID 22461567] Diabetes-associated common genetic variation and its association with GLP-1 concentrations and response to exogenous GLP-1.
[PMID 23107108] Lack of association between genetic polymorphisms within KCNQ1 locus and type 2 diabetes in Tunisian Arabs.
[PMID 28863213] Type 2 diabetes associated variants of KCNQ1 strongly confer the risk of cardiovascular disease among the Saudi Arabian population.