rs116855232
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;T) | 4 | Much higher (>10x) risk for leukopenia if treated with thiopurines |
| Make rs116855232(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 13 |
| Position | 48045719 |
| Gene | NUDT15 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs116855232 |
| dbSNP (classic) | rs116855232 |
| ClinGen | rs116855232 |
| ebi | rs116855232 |
| HLI | rs116855232 |
| Exac | rs116855232 |
| Gnomad | rs116855232 |
| Varsome | rs116855232 |
| LitVar | rs116855232 |
| Map | rs116855232 |
| PheGenI | rs116855232 |
| Biobank | rs116855232 |
| 1000 genomes | rs116855232 |
| hgdp | rs116855232 |
| ensembl | rs116855232 |
| geneview | rs116855232 |
| scholar | rs116855232 |
| rs116855232 | |
| pharmgkb | rs116855232 |
| gwascentral | rs116855232 |
| openSNP | rs116855232 |
| 23andMe | rs116855232 |
| SNPshot | rs116855232 |
| SNPdbe | rs116855232 |
| MSV3d | rs116855232 |
| GWAS Ctlg | rs116855232 |
| Max Magnitude | 4 |
c.415C>T, p.Arg139Cys, R139C; associated with poor response to azathioprine and mercaptopurine
The rs116855232(T) allele was strongly associated with thiopurine-induced early leukopenia (OR 35.6, p = 4.88 × 10e-94), based on a study of ~1000 Koreans, where this variant demonstrated sensitivity and specificity of 89.4% and 93.2%, respectively, for thiopurine-induced early leukopenia. This SNP was also strongly associated with thiopurine-induced leukopenia in subjects with inflammatory bowel disease of European descent (OR 9.5, p = 4.64 × 10e-4).[PMID 25108385
]
| ClinVar | |
|---|---|
| Risk | rs116855232(T;T) |
| Alt | rs116855232(T;T) |
| Reference | Rs116855232(C;C) |
| Significance | Drug-response |
| Disease | Thiopurines mercaptopurine response - Dosage azathioprine response - Dosage |
| Variation | info |
| Gene | NUDT15 |
| CLNDBN | Thiopurines, poor metabolism of, 2 mercaptopurine response - Dosage, Toxicity/ADR azathioprine response - Dosage, Toxicity/ADR |
| Reversed | 0 |
| HGVS | NC_000013.10:g.48619855C>T |
| CLNSRC | OMIM Allelic Variant PharmGKB Clinical Annotation |
| CLNACC | RCV000210853.1, RCV000211238.1, RCV000211416.1, |
