rs201663231
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs201663231(C;G) |
| Make rs201663231(G;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 10 |
| Position | 99714620 |
| Gene | COX15 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs201663231 |
| dbSNP (classic) | rs201663231 |
| ClinGen | rs201663231 |
| ebi | rs201663231 |
| HLI | rs201663231 |
| Exac | rs201663231 |
| Gnomad | rs201663231 |
| Varsome | rs201663231 |
| LitVar | rs201663231 |
| Map | rs201663231 |
| PheGenI | rs201663231 |
| Biobank | rs201663231 |
| 1000 genomes | rs201663231 |
| hgdp | rs201663231 |
| ensembl | rs201663231 |
| geneview | rs201663231 |
| scholar | rs201663231 |
| rs201663231 | |
| pharmgkb | rs201663231 |
| gwascentral | rs201663231 |
| openSNP | rs201663231 |
| 23andMe | rs201663231 |
| SNPshot | rs201663231 |
| SNPdbe | rs201663231 |
| MSV3d | rs201663231 |
| GWAS Ctlg | rs201663231 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs201663231(G;G) |
| Alt | rs201663231(G;G) |
| Reference | Rs201663231(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | COX15 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000010.10:g.101474377C>G |
| CLNSRC | |
| CLNACC | RCV000195737.2, |
