rs67294956
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs67294956(-;-) |
| Make rs67294956(-;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 38403660 |
| Gene | OTC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs67294956 |
| dbSNP (classic) | rs67294956 |
| ClinGen | rs67294956 |
| ebi | rs67294956 |
| HLI | rs67294956 |
| Exac | rs67294956 |
| Gnomad | rs67294956 |
| Varsome | rs67294956 |
| LitVar | rs67294956 |
| Map | rs67294956 |
| PheGenI | rs67294956 |
| Biobank | rs67294956 |
| 1000 genomes | rs67294956 |
| hgdp | rs67294956 |
| ensembl | rs67294956 |
| geneview | rs67294956 |
| scholar | rs67294956 |
| rs67294956 | |
| pharmgkb | rs67294956 |
| gwascentral | rs67294956 |
| openSNP | rs67294956 |
| 23andMe | rs67294956 |
| SNPshot | rs67294956 |
| SNPdbe | rs67294956 |
| MSV3d | rs67294956 |
| GWAS Ctlg | rs67294956 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs67294956(-;-) |
| Alt | rs67294956(-;-) |
| Reference | Rs67294956(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | OTC |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000023.10:g.38262913delG |
| CLNSRC | ClinVar |
| CLNACC | RCV000083498.1, |
