rs769031989
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs769031989(A;A) |
| Make rs769031989(A;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 17 |
| Position | 42322464 |
| Gene | STAT3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs769031989 |
| dbSNP (classic) | rs769031989 |
| ClinGen | rs769031989 |
| ebi | rs769031989 |
| HLI | rs769031989 |
| Exac | rs769031989 |
| Gnomad | rs769031989 |
| Varsome | rs769031989 |
| LitVar | rs769031989 |
| Map | rs769031989 |
| PheGenI | rs769031989 |
| Biobank | rs769031989 |
| 1000 genomes | rs769031989 |
| hgdp | rs769031989 |
| ensembl | rs769031989 |
| geneview | rs769031989 |
| scholar | rs769031989 |
| rs769031989 | |
| pharmgkb | rs769031989 |
| gwascentral | rs769031989 |
| openSNP | rs769031989 |
| 23andMe | rs769031989 |
| SNPshot | rs769031989 |
| SNPdbe | rs769031989 |
| MSV3d | rs769031989 |
| GWAS Ctlg | rs769031989 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs769031989(A;A) |
| Alt | rs769031989(A;A) |
| Reference | Rs769031989(T;T) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | STAT3 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000017.10:g.40474482T>A |
| CLNSRC | |
| CLNACC | RCV000414550.1, |
