rs121912195
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;T) | 3 | Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation |
| (T;T) | 0 | common/normal |
| Make rs121912195(C;C) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 11 |
| Position | 71442349 |
| Gene | DHCR7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs121912195 |
| dbSNP (classic) | rs121912195 |
| ClinGen | rs121912195 |
| ebi | rs121912195 |
| HLI | rs121912195 |
| Exac | rs121912195 |
| Gnomad | rs121912195 |
| Varsome | rs121912195 |
| LitVar | rs121912195 |
| Map | rs121912195 |
| PheGenI | rs121912195 |
| Biobank | rs121912195 |
| 1000 genomes | rs121912195 |
| hgdp | rs121912195 |
| ensembl | rs121912195 |
| geneview | rs121912195 |
| scholar | rs121912195 |
| rs121912195 | |
| pharmgkb | rs121912195 |
| gwascentral | rs121912195 |
| openSNP | rs121912195 |
| 23andMe | rs121912195 |
| SNPshot | rs121912195 |
| SNPdbe | rs121912195 |
| MSV3d | rs121912195 |
| GWAS Ctlg | rs121912195 |
| Max Magnitude | 3 |
