rs774202259
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs774202259(C;T) |
| Make rs774202259(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 19 |
| Position | 17843777 |
| Gene | JAK3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs774202259 |
| dbSNP (classic) | rs774202259 |
| ClinGen | rs774202259 |
| ebi | rs774202259 |
| HLI | rs774202259 |
| Exac | rs774202259 |
| Gnomad | rs774202259 |
| Varsome | rs774202259 |
| LitVar | rs774202259 |
| Map | rs774202259 |
| PheGenI | rs774202259 |
| Biobank | rs774202259 |
| 1000 genomes | rs774202259 |
| hgdp | rs774202259 |
| ensembl | rs774202259 |
| geneview | rs774202259 |
| scholar | rs774202259 |
| rs774202259 | |
| pharmgkb | rs774202259 |
| gwascentral | rs774202259 |
| openSNP | rs774202259 |
| 23andMe | rs774202259 |
| SNPshot | rs774202259 |
| SNPdbe | rs774202259 |
| MSV3d | rs774202259 |
| GWAS Ctlg | rs774202259 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs774202259(T;T) |
| Alt | rs774202259(T;T) |
| Reference | Rs774202259(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | JAK3 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000019.9:g.17954586C>T |
| CLNSRC | |
| CLNACC | RCV000171281.1, |
