rs766299724
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 3 | Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation |
| Make rs766299724(A;A) |
| Make rs766299724(G;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 11 |
| Position | 71441278 |
| Gene | DHCR7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs766299724 |
| dbSNP (classic) | rs766299724 |
| ClinGen | rs766299724 |
| ebi | rs766299724 |
| HLI | rs766299724 |
| Exac | rs766299724 |
| Gnomad | rs766299724 |
| Varsome | rs766299724 |
| LitVar | rs766299724 |
| Map | rs766299724 |
| PheGenI | rs766299724 |
| Biobank | rs766299724 |
| 1000 genomes | rs766299724 |
| hgdp | rs766299724 |
| ensembl | rs766299724 |
| geneview | rs766299724 |
| scholar | rs766299724 |
| rs766299724 | |
| pharmgkb | rs766299724 |
| gwascentral | rs766299724 |
| openSNP | rs766299724 |
| 23andMe | rs766299724 |
| SNPshot | rs766299724 |
| SNPdbe | rs766299724 |
| MSV3d | rs766299724 |
| GWAS Ctlg | rs766299724 |
| Max Magnitude | 3 |
