rs202052174
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs202052174(A;A) |
| Make rs202052174(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 10 |
| Position | 71803371 |
| Gene | CDH23 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs202052174 |
| dbSNP (classic) | rs202052174 |
| ClinGen | rs202052174 |
| ebi | rs202052174 |
| HLI | rs202052174 |
| Exac | rs202052174 |
| Gnomad | rs202052174 |
| Varsome | rs202052174 |
| LitVar | rs202052174 |
| Map | rs202052174 |
| PheGenI | rs202052174 |
| Biobank | rs202052174 |
| 1000 genomes | rs202052174 |
| hgdp | rs202052174 |
| ensembl | rs202052174 |
| geneview | rs202052174 |
| scholar | rs202052174 |
| rs202052174 | |
| pharmgkb | rs202052174 |
| gwascentral | rs202052174 |
| openSNP | rs202052174 |
| 23andMe | rs202052174 |
| SNPshot | rs202052174 |
| SNPdbe | rs202052174 |
| MSV3d | rs202052174 |
| GWAS Ctlg | rs202052174 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs202052174(A;A) |
| Alt | rs202052174(A;A) |
| Reference | Rs202052174(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | CDH23 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000010.10:g.73563128G>A |
| CLNSRC | ClinVar |
| CLNACC | RCV000039276.4, |
