rs769688376
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs769688376(A;A) |
| Make rs769688376(A;C) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 19 |
| Position | 36089289 |
| Gene | WDR62 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs769688376 |
| dbSNP (classic) | rs769688376 |
| ClinGen | rs769688376 |
| ebi | rs769688376 |
| HLI | rs769688376 |
| Exac | rs769688376 |
| Gnomad | rs769688376 |
| Varsome | rs769688376 |
| LitVar | rs769688376 |
| Map | rs769688376 |
| PheGenI | rs769688376 |
| Biobank | rs769688376 |
| 1000 genomes | rs769688376 |
| hgdp | rs769688376 |
| ensembl | rs769688376 |
| geneview | rs769688376 |
| scholar | rs769688376 |
| rs769688376 | |
| pharmgkb | rs769688376 |
| gwascentral | rs769688376 |
| openSNP | rs769688376 |
| 23andMe | rs769688376 |
| SNPshot | rs769688376 |
| SNPdbe | rs769688376 |
| MSV3d | rs769688376 |
| GWAS Ctlg | rs769688376 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs769688376(A;A) |
| Alt | rs769688376(A;A) |
| Reference | Rs769688376(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | WDR62 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000019.9:g.36580191C>A |
| CLNSRC | |
| CLNACC | RCV000330039.1, |
