rs191486604
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs191486604(A;A) |
| Make rs191486604(A;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 6 |
| Position | 161350208 |
| Gene | PARK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs191486604 |
| dbSNP (classic) | rs191486604 |
| ClinGen | rs191486604 |
| ebi | rs191486604 |
| HLI | rs191486604 |
| Exac | rs191486604 |
| Gnomad | rs191486604 |
| Varsome | rs191486604 |
| LitVar | rs191486604 |
| Map | rs191486604 |
| PheGenI | rs191486604 |
| Biobank | rs191486604 |
| 1000 genomes | rs191486604 |
| hgdp | rs191486604 |
| ensembl | rs191486604 |
| geneview | rs191486604 |
| scholar | rs191486604 |
| rs191486604 | |
| pharmgkb | rs191486604 |
| gwascentral | rs191486604 |
| openSNP | rs191486604 |
| 23andMe | rs191486604 |
| SNPshot | rs191486604 |
| SNPdbe | rs191486604 |
| MSV3d | rs191486604 |
| GWAS Ctlg | rs191486604 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs191486604(A;A) |
| Alt | rs191486604(A;A) |
| Reference | Rs191486604(G;G) |
| Significance | Probable-Pathogenic |
| Disease | Parkinson Disease |
| Variation | info |
| Gene | PARK2 |
| CLNDBN | Parkinson Disease, Juvenile |
| Reversed | 1 |
| HGVS | NC_000006.11:g.161771240C>T |
| CLNSRC | Illumina |
| CLNACC | RCV000269607.1, |
