rs7957197
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 |
Make rs7957197(A;A) |
Make rs7957197(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 121022883 |
Gene | OASL |
is a | snp |
is | mentioned by |
dbSNP | rs7957197 |
dbSNP (classic) | rs7957197 |
ClinGen | rs7957197 |
ebi | rs7957197 |
HLI | rs7957197 |
Exac | rs7957197 |
Gnomad | rs7957197 |
Varsome | rs7957197 |
LitVar | rs7957197 |
Map | rs7957197 |
PheGenI | rs7957197 |
Biobank | rs7957197 |
1000 genomes | rs7957197 |
hgdp | rs7957197 |
ensembl | rs7957197 |
geneview | rs7957197 |
scholar | rs7957197 |
rs7957197 | |
pharmgkb | rs7957197 |
gwascentral | rs7957197 |
openSNP | rs7957197 |
23andMe | rs7957197 |
SNPshot | rs7957197 |
SNPdbe | rs7957197 |
MSV3d | rs7957197 |
GWAS Ctlg | rs7957197 |
GMAF | 0.1313 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20581827] |
Trait | Type 2 diabetes |
Title | Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis |
Risk Allele | T |
P-val | 2E-8 |
Odds Ratio | 1.07 [1.05-1.10] |
[PMID 21278902] Genetic risk profiling for prediction of type 2 diabetes.
[PMID 22996131] Monogenic models: what have the single gene disorders taught us?
[PMID 23462794] Identification of CpG-SNPs associated with type 2 diabetes and differential DNA methylation in human pancreatic islets.