rs763670293
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs763670293(C;T) |
| Make rs763670293(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 5 |
| Position | 90728720 |
| Gene | ADGRV1, LOC105379077 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs763670293 |
| dbSNP (classic) | rs763670293 |
| ClinGen | rs763670293 |
| ebi | rs763670293 |
| HLI | rs763670293 |
| Exac | rs763670293 |
| Gnomad | rs763670293 |
| Varsome | rs763670293 |
| LitVar | rs763670293 |
| Map | rs763670293 |
| PheGenI | rs763670293 |
| Biobank | rs763670293 |
| 1000 genomes | rs763670293 |
| hgdp | rs763670293 |
| ensembl | rs763670293 |
| geneview | rs763670293 |
| scholar | rs763670293 |
| rs763670293 | |
| pharmgkb | rs763670293 |
| gwascentral | rs763670293 |
| openSNP | rs763670293 |
| 23andMe | rs763670293 |
| SNPshot | rs763670293 |
| SNPdbe | rs763670293 |
| MSV3d | rs763670293 |
| GWAS Ctlg | rs763670293 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs763670293(T;T) |
| Alt | rs763670293(T;T) |
| Reference | Rs763670293(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ADGRV1 GPR98 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000005.9:g.90024537C>T |
| CLNSRC | |
| CLNACC | RCV000255292.1, |
