rs390802
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs390802(A;A) |
| Make rs390802(A;G) |
| Make rs390802(G;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 3 |
| Position | 52397655 |
| Gene | DNAH1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs390802 |
| dbSNP (classic) | rs390802 |
| ClinGen | rs390802 |
| ebi | rs390802 |
| HLI | rs390802 |
| Exac | rs390802 |
| Gnomad | rs390802 |
| Varsome | rs390802 |
| LitVar | rs390802 |
| Map | rs390802 |
| PheGenI | rs390802 |
| Biobank | rs390802 |
| 1000 genomes | rs390802 |
| hgdp | rs390802 |
| ensembl | rs390802 |
| geneview | rs390802 |
| scholar | rs390802 |
| rs390802 | |
| pharmgkb | rs390802 |
| gwascentral | rs390802 |
| openSNP | rs390802 |
| 23andMe | rs390802 |
| SNPshot | rs390802 |
| SNPdbe | rs390802 |
| MSV3d | rs390802 |
| GWAS Ctlg | rs390802 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 29088836
] Common, germline genetic variations in the novel tumor suppressor BAP1 and risk of developing different types of cancer.
