rs568165874
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs568165874(C;T) |
| Make rs568165874(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 12 |
| Position | 57763738 |
| Gene | CYP27B1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs568165874 |
| dbSNP (classic) | rs568165874 |
| ClinGen | rs568165874 |
| ebi | rs568165874 |
| HLI | rs568165874 |
| Exac | rs568165874 |
| Gnomad | rs568165874 |
| Varsome | rs568165874 |
| LitVar | rs568165874 |
| Map | rs568165874 |
| PheGenI | rs568165874 |
| Biobank | rs568165874 |
| 1000 genomes | rs568165874 |
| hgdp | rs568165874 |
| ensembl | rs568165874 |
| geneview | rs568165874 |
| scholar | rs568165874 |
| rs568165874 | |
| pharmgkb | rs568165874 |
| gwascentral | rs568165874 |
| openSNP | rs568165874 |
| 23andMe | rs568165874 |
| SNPshot | rs568165874 |
| SNPdbe | rs568165874 |
| MSV3d | rs568165874 |
| GWAS Ctlg | rs568165874 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs568165874(G;G) rs568165874(T;T) |
| Alt | rs568165874(G;G) rs568165874(T;T) |
| Reference | Rs568165874(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | CYP27B1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000012.11:g.58157521C>G |
| CLNSRC | |
| CLNACC | RCV000255484.1, |
