rs3746876
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs3746876(C;T) |
Make rs3746876(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 38299525 |
Gene | KCNJ15 |
is a | snp |
is | mentioned by |
dbSNP | rs3746876 |
dbSNP (classic) | rs3746876 |
ClinGen | rs3746876 |
ebi | rs3746876 |
HLI | rs3746876 |
Exac | rs3746876 |
Gnomad | rs3746876 |
Varsome | rs3746876 |
LitVar | rs3746876 |
Map | rs3746876 |
PheGenI | rs3746876 |
Biobank | rs3746876 |
1000 genomes | rs3746876 |
hgdp | rs3746876 |
ensembl | rs3746876 |
geneview | rs3746876 |
scholar | rs3746876 |
rs3746876 | |
pharmgkb | rs3746876 |
gwascentral | rs3746876 |
openSNP | rs3746876 |
23andMe | rs3746876 |
SNPshot | rs3746876 |
SNPdbe | rs3746876 |
MSV3d | rs3746876 |
GWAS Ctlg | rs3746876 |
GMAF | 0.04591 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20085713] Identification of KCNJ15 as a Susceptibility Gene in Asian Patients with Type 2 Diabetes Mellitus
OMIM | 602106 |
Desc | POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 15; KCNJ15 |
Variant | |
Related | also |
[PMID 23595124] Replication study for the association of a single-nucleotide polymorphism, rs3746876, within KCNJ15, with susceptibility to type 2 diabetes in a Japanese population