rs74423290
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs74423290(C;G) |
| Make rs74423290(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 18133884 |
| Gene | TPMT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs74423290 |
| dbSNP (classic) | rs74423290 |
| ClinGen | rs74423290 |
| ebi | rs74423290 |
| HLI | rs74423290 |
| Exac | rs74423290 |
| Gnomad | rs74423290 |
| Varsome | rs74423290 |
| LitVar | rs74423290 |
| Map | rs74423290 |
| PheGenI | rs74423290 |
| Biobank | rs74423290 |
| 1000 genomes | rs74423290 |
| hgdp | rs74423290 |
| ensembl | rs74423290 |
| geneview | rs74423290 |
| scholar | rs74423290 |
| rs74423290 | |
| pharmgkb | rs74423290 |
| gwascentral | rs74423290 |
| openSNP | rs74423290 |
| 23andMe | rs74423290 |
| SNPshot | rs74423290 |
| SNPdbe | rs74423290 |
| MSV3d | rs74423290 |
| GWAS Ctlg | rs74423290 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs74423290(G;G) |
| Alt | rs74423290(G;G) |
| Reference | Rs74423290(C;C) |
| Significance | Drug-response |
| Disease | Thiopurine methyltransferase deficiency |
| Variation | info |
| Gene | TPMT |
| CLNDBN | Thiopurine methyltransferase deficiency |
| Reversed | 1 |
| HGVS | NC_000006.11:g.18134115G>C |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000013564.25, |
