rs765249238
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs765249238(C;T) |
| Make rs765249238(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 3 |
| Position | 133948892 |
| Gene | SLCO2A1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs765249238 |
| dbSNP (classic) | rs765249238 |
| ClinGen | rs765249238 |
| ebi | rs765249238 |
| HLI | rs765249238 |
| Exac | rs765249238 |
| Gnomad | rs765249238 |
| Varsome | rs765249238 |
| LitVar | rs765249238 |
| Map | rs765249238 |
| PheGenI | rs765249238 |
| Biobank | rs765249238 |
| 1000 genomes | rs765249238 |
| hgdp | rs765249238 |
| ensembl | rs765249238 |
| geneview | rs765249238 |
| scholar | rs765249238 |
| rs765249238 | |
| pharmgkb | rs765249238 |
| gwascentral | rs765249238 |
| openSNP | rs765249238 |
| 23andMe | rs765249238 |
| SNPshot | rs765249238 |
| SNPdbe | rs765249238 |
| MSV3d | rs765249238 |
| GWAS Ctlg | rs765249238 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs765249238(T;T) |
| Alt | rs765249238(T;T) |
| Reference | Rs765249238(C;C) |
| Significance | Pathogenic |
| Disease | Primary hypertrophic osteoarthropathy |
| Variation | info |
| Gene | SLCO2A1 |
| CLNDBN | Primary hypertrophic osteoarthropathy, autosomal recessive 2 |
| Reversed | 0 |
| HGVS | NC_000003.11:g.133667736C>T |
| CLNSRC | |
| CLNACC | RCV000490351.1, |
