rs763982675
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs763982675(A;A) |
| Make rs763982675(A;C) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 7 |
| Position | 138747514 |
| Gene | ATP6V0A4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs763982675 |
| dbSNP (classic) | rs763982675 |
| ClinGen | rs763982675 |
| ebi | rs763982675 |
| HLI | rs763982675 |
| Exac | rs763982675 |
| Gnomad | rs763982675 |
| Varsome | rs763982675 |
| LitVar | rs763982675 |
| Map | rs763982675 |
| PheGenI | rs763982675 |
| Biobank | rs763982675 |
| 1000 genomes | rs763982675 |
| hgdp | rs763982675 |
| ensembl | rs763982675 |
| geneview | rs763982675 |
| scholar | rs763982675 |
| rs763982675 | |
| pharmgkb | rs763982675 |
| gwascentral | rs763982675 |
| openSNP | rs763982675 |
| 23andMe | rs763982675 |
| SNPshot | rs763982675 |
| SNPdbe | rs763982675 |
| MSV3d | rs763982675 |
| GWAS Ctlg | rs763982675 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs763982675(A;A) |
| Alt | rs763982675(A;A) |
| Reference | Rs763982675(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ATP6V0A4 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000007.13:g.138432259C>A |
| CLNSRC | |
| CLNACC | RCV000442300.1, |
