rs9976767
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9976767(A;A) |
| Make rs9976767(A;G) |
| Make rs9976767(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 42416281 |
| Gene | UBASH3A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9976767 |
| dbSNP (classic) | rs9976767 |
| ClinGen | rs9976767 |
| ebi | rs9976767 |
| HLI | rs9976767 |
| Exac | rs9976767 |
| Gnomad | rs9976767 |
| Varsome | rs9976767 |
| LitVar | rs9976767 |
| Map | rs9976767 |
| PheGenI | rs9976767 |
| Biobank | rs9976767 |
| 1000 genomes | rs9976767 |
| hgdp | rs9976767 |
| ensembl | rs9976767 |
| geneview | rs9976767 |
| scholar | rs9976767 |
| rs9976767 | |
| pharmgkb | rs9976767 |
| gwascentral | rs9976767 |
| openSNP | rs9976767 |
| 23andMe | rs9976767 |
| SNPshot | rs9976767 |
| SNPdbe | rs9976767 |
| MSV3d | rs9976767 |
| GWAS Ctlg | rs9976767 |
| GMAF | 0.4201 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 18840781 ]
|
| Trait | Type 1 diabetes |
| Title | Follow up analysis of genome-wide association data identifies novel loci for type 1 diabetes |
| Risk Allele | C |
| P-val | 2E-8 |
| Odds Ratio | 1.16 [1.10-1.22] |
