rs202033121
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs202033121(A;A) |
| Make rs202033121(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 10 |
| Position | 53938872 |
| Gene | PCDH15 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs202033121 |
| dbSNP (classic) | rs202033121 |
| ClinGen | rs202033121 |
| ebi | rs202033121 |
| HLI | rs202033121 |
| Exac | rs202033121 |
| Gnomad | rs202033121 |
| Varsome | rs202033121 |
| LitVar | rs202033121 |
| Map | rs202033121 |
| PheGenI | rs202033121 |
| Biobank | rs202033121 |
| 1000 genomes | rs202033121 |
| hgdp | rs202033121 |
| ensembl | rs202033121 |
| geneview | rs202033121 |
| scholar | rs202033121 |
| rs202033121 | |
| pharmgkb | rs202033121 |
| gwascentral | rs202033121 |
| openSNP | rs202033121 |
| 23andMe | rs202033121 |
| SNPshot | rs202033121 |
| SNPdbe | rs202033121 |
| MSV3d | rs202033121 |
| GWAS Ctlg | rs202033121 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs202033121(A;A) |
| Alt | rs202033121(A;A) |
| Reference | Rs202033121(G;G) |
| Significance | Other |
| Disease | Usher syndrome |
| Variation | info |
| Gene | PCDH15 |
| CLNDBN | Usher syndrome, type 1F |
| Reversed | 0 |
| HGVS | NC_000010.10:g.55698632G>A |
| CLNSRC | ClinVar |
| CLNACC | RCV000039723.4, |
