rs371981035
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs371981035(A;G) |
| Make rs371981035(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 90810231 |
| Gene | ADGRV1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs371981035 |
| dbSNP (classic) | rs371981035 |
| ClinGen | rs371981035 |
| ebi | rs371981035 |
| HLI | rs371981035 |
| Exac | rs371981035 |
| Gnomad | rs371981035 |
| Varsome | rs371981035 |
| LitVar | rs371981035 |
| Map | rs371981035 |
| PheGenI | rs371981035 |
| Biobank | rs371981035 |
| 1000 genomes | rs371981035 |
| hgdp | rs371981035 |
| ensembl | rs371981035 |
| geneview | rs371981035 |
| scholar | rs371981035 |
| rs371981035 | |
| pharmgkb | rs371981035 |
| gwascentral | rs371981035 |
| openSNP | rs371981035 |
| 23andMe | rs371981035 |
| SNPshot | rs371981035 |
| SNPdbe | rs371981035 |
| MSV3d | rs371981035 |
| GWAS Ctlg | rs371981035 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs371981035(G;G) |
| Alt | rs371981035(G;G) |
| Reference | Rs371981035(A;A) |
| Significance | Pathogenic |
| Disease | Usher syndrome |
| Variation | info |
| Gene | ADGRV1 GPR98 |
| CLNDBN | Usher syndrome, type 2C |
| Reversed | 0 |
| HGVS | NC_000005.9:g.90106048A>G |
| CLNSRC | ClinVar |
| CLNACC | RCV000039531.2, |
