rs104893997
From SNPedia
| Merged into | rs1800454 |
| Orientation | minus |
| Stabilized | minus |
| Make rs104893997(A;A) |
| Make rs104893997(A;G) |
| Make rs104893997(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32832635 |
| Gene | TAP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs104893997 |
| dbSNP (classic) | rs104893997 |
| ClinGen | rs104893997 |
| ebi | rs104893997 |
| HLI | rs104893997 |
| Exac | rs104893997 |
| Gnomad | rs104893997 |
| Varsome | rs104893997 |
| LitVar | rs104893997 |
| Map | rs104893997 |
| PheGenI | rs104893997 |
| Biobank | rs104893997 |
| 1000 genomes | rs104893997 |
| hgdp | rs104893997 |
| ensembl | rs104893997 |
| geneview | rs104893997 |
| scholar | rs104893997 |
| rs104893997 | |
| pharmgkb | rs104893997 |
| gwascentral | rs104893997 |
| openSNP | rs104893997 |
| 23andMe | rs104893997 |
| SNPshot | rs104893997 |
| SNPdbe | rs104893997 |
| MSV3d | rs104893997 |
| GWAS Ctlg | rs104893997 |
| Status | Merged into rs1800454 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
