rs535561852
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 3 | Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation |
| (G;G) | 0 | common/normal |
| Make rs535561852(A;A) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 11 |
| Position | 71435476 |
| Gene | DHCR7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs535561852 |
| dbSNP (classic) | rs535561852 |
| ClinGen | rs535561852 |
| ebi | rs535561852 |
| HLI | rs535561852 |
| Exac | rs535561852 |
| Gnomad | rs535561852 |
| Varsome | rs535561852 |
| LitVar | rs535561852 |
| Map | rs535561852 |
| PheGenI | rs535561852 |
| Biobank | rs535561852 |
| 1000 genomes | rs535561852 |
| hgdp | rs535561852 |
| ensembl | rs535561852 |
| geneview | rs535561852 |
| scholar | rs535561852 |
| rs535561852 | |
| pharmgkb | rs535561852 |
| gwascentral | rs535561852 |
| openSNP | rs535561852 |
| 23andMe | rs535561852 |
| SNPshot | rs535561852 |
| SNPdbe | rs535561852 |
| MSV3d | rs535561852 |
| GWAS Ctlg | rs535561852 |
| Max Magnitude | 3 |
