rs104886033
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| (A;G) | 3 | Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation |
| Make rs104886033(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 71444952 |
| Gene | DHCR7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs104886033 |
| dbSNP (classic) | rs104886033 |
| ClinGen | rs104886033 |
| ebi | rs104886033 |
| HLI | rs104886033 |
| Exac | rs104886033 |
| Gnomad | rs104886033 |
| Varsome | rs104886033 |
| LitVar | rs104886033 |
| Map | rs104886033 |
| PheGenI | rs104886033 |
| Biobank | rs104886033 |
| 1000 genomes | rs104886033 |
| hgdp | rs104886033 |
| ensembl | rs104886033 |
| geneview | rs104886033 |
| scholar | rs104886033 |
| rs104886033 | |
| pharmgkb | rs104886033 |
| gwascentral | rs104886033 |
| openSNP | rs104886033 |
| 23andMe | rs104886033 |
| SNPshot | rs104886033 |
| SNPdbe | rs104886033 |
| MSV3d | rs104886033 |
| GWAS Ctlg | rs104886033 |
| Max Magnitude | 3 |
| ClinVar | |
|---|---|
| Risk | rs104886033(G;G) |
| Alt | rs104886033(G;G) |
| Reference | Rs104886033(A;A) |
| Significance | Other |
| Disease | Smith-Lemli-Opitz syndrome not provided |
| Variation | info |
| Gene | DHCR7 |
| CLNDBN | Smith-Lemli-Opitz syndrome not provided |
| Reversed | 1 |
| HGVS | NC_000011.9:g.71155998T>C |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000169384.2, RCV000224026.1, |
[PMID 15776424] Identification of 14 novel mutations in DHCR7 causing the Smith-Lemli-Opitz syndrome and delineation of the DHCR7 mutational spectra in Spain and Italy.
