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.
