rs186364861
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs186364861(A;A) |
| Make rs186364861(A;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 13 |
| Position | 48037798 |
| Gene | NUDT15, SUCLA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs186364861 |
| dbSNP (classic) | rs186364861 |
| ClinGen | rs186364861 |
| ebi | rs186364861 |
| HLI | rs186364861 |
| Exac | rs186364861 |
| Gnomad | rs186364861 |
| Varsome | rs186364861 |
| LitVar | rs186364861 |
| Map | rs186364861 |
| PheGenI | rs186364861 |
| Biobank | rs186364861 |
| 1000 genomes | rs186364861 |
| hgdp | rs186364861 |
| ensembl | rs186364861 |
| geneview | rs186364861 |
| scholar | rs186364861 |
| rs186364861 | |
| pharmgkb | rs186364861 |
| gwascentral | rs186364861 |
| openSNP | rs186364861 |
| 23andMe | rs186364861 |
| SNPshot | rs186364861 |
| SNPdbe | rs186364861 |
| MSV3d | rs186364861 |
| GWAS Ctlg | rs186364861 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs186364861(A;A) |
| Alt | rs186364861(A;A) |
| Reference | Rs186364861(G;G) |
| Significance | Drug-response |
| Disease | Thiopurines |
| Variation | info |
| Gene | NUDT15 SUCLA2 |
| CLNDBN | Thiopurines, poor metabolism of, 2 |
| Reversed | 0 |
| HGVS | NC_000013.10:g.48611934G>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000210850.1, |
