rs866754647
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs866754647(A;A) |
| Make rs866754647(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | X |
| Position | 83508971 |
| Gene | POU3F4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs866754647 |
| dbSNP (classic) | rs866754647 |
| ClinGen | rs866754647 |
| ebi | rs866754647 |
| HLI | rs866754647 |
| Exac | rs866754647 |
| Gnomad | rs866754647 |
| Varsome | rs866754647 |
| LitVar | rs866754647 |
| Map | rs866754647 |
| PheGenI | rs866754647 |
| Biobank | rs866754647 |
| 1000 genomes | rs866754647 |
| hgdp | rs866754647 |
| ensembl | rs866754647 |
| geneview | rs866754647 |
| scholar | rs866754647 |
| rs866754647 | |
| pharmgkb | rs866754647 |
| gwascentral | rs866754647 |
| openSNP | rs866754647 |
| 23andMe | rs866754647 |
| SNPshot | rs866754647 |
| SNPdbe | rs866754647 |
| MSV3d | rs866754647 |
| GWAS Ctlg | rs866754647 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs866754647(A;A) |
| Alt | rs866754647(A;A) |
| Reference | Rs866754647(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | POU3F4 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000023.10:g.82763979G>A |
| CLNSRC | |
| CLNACC | RCV000480190.1, |
