rs876498
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs876498(C;C) |
| Make rs876498(C;T) |
| Make rs876498(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 42421718 |
| Gene | UBASH3A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs876498 |
| dbSNP (classic) | rs876498 |
| ClinGen | rs876498 |
| ebi | rs876498 |
| HLI | rs876498 |
| Exac | rs876498 |
| Gnomad | rs876498 |
| Varsome | rs876498 |
| LitVar | rs876498 |
| Map | rs876498 |
| PheGenI | rs876498 |
| Biobank | rs876498 |
| 1000 genomes | rs876498 |
| hgdp | rs876498 |
| ensembl | rs876498 |
| geneview | rs876498 |
| scholar | rs876498 |
| rs876498 | |
| pharmgkb | rs876498 |
| gwascentral | rs876498 |
| openSNP | rs876498 |
| 23andMe | rs876498 |
| SNPshot | rs876498 |
| SNPdbe | rs876498 |
| MSV3d | rs876498 |
| GWAS Ctlg | rs876498 |
| GMAF | 0.4008 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 18647951
] type-1 diabetes rs876498 (P=1.0x10(-4))
[PMID 19073967] Shared and distinct genetic variants in type 1 diabetes and celiac disease.
[PMID 19732865] A generalized family-based association test for dichotomous traits.
