rs200529020
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs200529020(A;A) |
| Make rs200529020(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 10 |
| Position | 97598894 |
| Gene | HOGA1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs200529020 |
| dbSNP (classic) | rs200529020 |
| ClinGen | rs200529020 |
| ebi | rs200529020 |
| HLI | rs200529020 |
| Exac | rs200529020 |
| Gnomad | rs200529020 |
| Varsome | rs200529020 |
| LitVar | rs200529020 |
| Map | rs200529020 |
| PheGenI | rs200529020 |
| Biobank | rs200529020 |
| 1000 genomes | rs200529020 |
| hgdp | rs200529020 |
| ensembl | rs200529020 |
| geneview | rs200529020 |
| scholar | rs200529020 |
| rs200529020 | |
| pharmgkb | rs200529020 |
| gwascentral | rs200529020 |
| openSNP | rs200529020 |
| 23andMe | rs200529020 |
| SNPshot | rs200529020 |
| SNPdbe | rs200529020 |
| MSV3d | rs200529020 |
| GWAS Ctlg | rs200529020 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs200529020(A;A) |
| Alt | rs200529020(A;A) |
| Reference | Rs200529020(G;G) |
| Significance | Probable-Pathogenic |
| Disease | Primary hyperoxaluria |
| Variation | info |
| Gene | HOGA1 |
| CLNDBN | Primary hyperoxaluria, type III |
| Reversed | 0 |
| HGVS | NC_000010.10:g.99358651G>A |
| CLNSRC | |
| CLNACC | RCV000449564.1, |
