rs368269558
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common/normal |
| (C;T) | 3 | Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation |
| Make rs368269558(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 11 |
| Position | 71441330 |
| Gene | DHCR7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs368269558 |
| dbSNP (classic) | rs368269558 |
| ClinGen | rs368269558 |
| ebi | rs368269558 |
| HLI | rs368269558 |
| Exac | rs368269558 |
| Gnomad | rs368269558 |
| Varsome | rs368269558 |
| LitVar | rs368269558 |
| Map | rs368269558 |
| PheGenI | rs368269558 |
| Biobank | rs368269558 |
| 1000 genomes | rs368269558 |
| hgdp | rs368269558 |
| ensembl | rs368269558 |
| geneview | rs368269558 |
| scholar | rs368269558 |
| rs368269558 | |
| pharmgkb | rs368269558 |
| gwascentral | rs368269558 |
| openSNP | rs368269558 |
| 23andMe | rs368269558 |
| SNPshot | rs368269558 |
| SNPdbe | rs368269558 |
| MSV3d | rs368269558 |
| GWAS Ctlg | rs368269558 |
| Max Magnitude | 3 |
