rs776996552
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs776996552(C;T) |
| Make rs776996552(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 17 |
| Position | 38343441 |
| Gene | GPR179 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs776996552 |
| dbSNP (classic) | rs776996552 |
| ClinGen | rs776996552 |
| ebi | rs776996552 |
| HLI | rs776996552 |
| Exac | rs776996552 |
| Gnomad | rs776996552 |
| Varsome | rs776996552 |
| LitVar | rs776996552 |
| Map | rs776996552 |
| PheGenI | rs776996552 |
| Biobank | rs776996552 |
| 1000 genomes | rs776996552 |
| hgdp | rs776996552 |
| ensembl | rs776996552 |
| geneview | rs776996552 |
| scholar | rs776996552 |
| rs776996552 | |
| pharmgkb | rs776996552 |
| gwascentral | rs776996552 |
| openSNP | rs776996552 |
| 23andMe | rs776996552 |
| SNPshot | rs776996552 |
| SNPdbe | rs776996552 |
| MSV3d | rs776996552 |
| GWAS Ctlg | rs776996552 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs776996552(T;T) |
| Alt | rs776996552(T;T) |
| Reference | Rs776996552(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | GPR179 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000017.10:g.36499324C>T |
| CLNSRC | |
| CLNACC | RCV000171255.1, |
