rs767167623
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 7 | 3HSDB2 deficiency; congenital adrenal hyperplasia |
| (-;G) | 3 | Unaffected carrier of a 3HSDB2 deficiency mutation |
| (G;G) | 0 | common/normal |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 1 |
| Position | 119422368 |
| Gene | HSD3B2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs767167623 |
| dbSNP (classic) | rs767167623 |
| ClinGen | rs767167623 |
| ebi | rs767167623 |
| HLI | rs767167623 |
| Exac | rs767167623 |
| Gnomad | rs767167623 |
| Varsome | rs767167623 |
| LitVar | rs767167623 |
| Map | rs767167623 |
| PheGenI | rs767167623 |
| Biobank | rs767167623 |
| 1000 genomes | rs767167623 |
| hgdp | rs767167623 |
| ensembl | rs767167623 |
| geneview | rs767167623 |
| scholar | rs767167623 |
| rs767167623 | |
| pharmgkb | rs767167623 |
| gwascentral | rs767167623 |
| openSNP | rs767167623 |
| 23andMe | rs767167623 |
| SNPshot | rs767167623 |
| SNPdbe | rs767167623 |
| MSV3d | rs767167623 |
| GWAS Ctlg | rs767167623 |
| Max Magnitude | 7 |
rs767167623, also known as c.867delG, represents a rare mutation in the HSD3B2 gene on chromosome 1.
