rs761458977
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common/normal |
| (A;G) | 3 | Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation |
| Make rs761458977(G;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 11 |
| Position | 71435452 |
| Gene | DHCR7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs761458977 |
| dbSNP (classic) | rs761458977 |
| ClinGen | rs761458977 |
| ebi | rs761458977 |
| HLI | rs761458977 |
| Exac | rs761458977 |
| Gnomad | rs761458977 |
| Varsome | rs761458977 |
| LitVar | rs761458977 |
| Map | rs761458977 |
| PheGenI | rs761458977 |
| Biobank | rs761458977 |
| 1000 genomes | rs761458977 |
| hgdp | rs761458977 |
| ensembl | rs761458977 |
| geneview | rs761458977 |
| scholar | rs761458977 |
| rs761458977 | |
| pharmgkb | rs761458977 |
| gwascentral | rs761458977 |
| openSNP | rs761458977 |
| 23andMe | rs761458977 |
| SNPshot | rs761458977 |
| SNPdbe | rs761458977 |
| MSV3d | rs761458977 |
| GWAS Ctlg | rs761458977 |
| Max Magnitude | 3 |
