rs765849229
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs765849229(A;A) |
| Make rs765849229(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 5 |
| Position | 90791195 |
| Gene | ADGRV1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs765849229 |
| dbSNP (classic) | rs765849229 |
| ClinGen | rs765849229 |
| ebi | rs765849229 |
| HLI | rs765849229 |
| Exac | rs765849229 |
| Gnomad | rs765849229 |
| Varsome | rs765849229 |
| LitVar | rs765849229 |
| Map | rs765849229 |
| PheGenI | rs765849229 |
| Biobank | rs765849229 |
| 1000 genomes | rs765849229 |
| hgdp | rs765849229 |
| ensembl | rs765849229 |
| geneview | rs765849229 |
| scholar | rs765849229 |
| rs765849229 | |
| pharmgkb | rs765849229 |
| gwascentral | rs765849229 |
| openSNP | rs765849229 |
| 23andMe | rs765849229 |
| SNPshot | rs765849229 |
| SNPdbe | rs765849229 |
| MSV3d | rs765849229 |
| GWAS Ctlg | rs765849229 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs765849229(A;A) |
| Alt | rs765849229(A;A) |
| Reference | Rs765849229(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | GPR98 ADGRV1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000005.9:g.90087012G>A |
| CLNSRC | |
| CLNACC | RCV000482131.1, |
