rs9332969
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs9332969(A;A) |
| Make rs9332969(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 67722899 |
| Gene | AR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9332969 |
| dbSNP (classic) | rs9332969 |
| ClinGen | rs9332969 |
| ebi | rs9332969 |
| HLI | rs9332969 |
| Exac | rs9332969 |
| Gnomad | rs9332969 |
| Varsome | rs9332969 |
| LitVar | rs9332969 |
| Map | rs9332969 |
| PheGenI | rs9332969 |
| Biobank | rs9332969 |
| 1000 genomes | rs9332969 |
| hgdp | rs9332969 |
| ensembl | rs9332969 |
| geneview | rs9332969 |
| scholar | rs9332969 |
| rs9332969 | |
| pharmgkb | rs9332969 |
| gwascentral | rs9332969 |
| openSNP | rs9332969 |
| 23andMe | rs9332969 |
| SNPshot | rs9332969 |
| SNPdbe | rs9332969 |
| MSV3d | rs9332969 |
| GWAS Ctlg | rs9332969 |
| Max Magnitude | 0 |
| ? | (A;G) (G;G) | |
|---|---|---|
|
| ||
| ClinVar | |
|---|---|
| Risk | rs9332969(A;A) |
| Alt | rs9332969(A;A) |
| Reference | Rs9332969(G;G) |
| Significance | Pathogenic |
| Disease | Reifenstein syndrome |
| Variation | info |
| Gene | AR |
| CLNDBN | Reifenstein syndrome |
| Reversed | 0 |
| HGVS | NC_000023.10:g.66942741G>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000010503.2, |
