rs74315356
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 8.9 | Parkinson's disease, type 6, early-onset |
| (A;G) | 3 | Carrier of an early-onset Parkinson's mutation |
| (G;G) | 0 | common in clinvar |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 20649054 |
| Gene | PINK1, PINK1-AS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs74315356 |
| dbSNP (classic) | rs74315356 |
| ClinGen | rs74315356 |
| ebi | rs74315356 |
| HLI | rs74315356 |
| Exac | rs74315356 |
| Gnomad | rs74315356 |
| Varsome | rs74315356 |
| LitVar | rs74315356 |
| Map | rs74315356 |
| PheGenI | rs74315356 |
| Biobank | rs74315356 |
| 1000 genomes | rs74315356 |
| hgdp | rs74315356 |
| ensembl | rs74315356 |
| geneview | rs74315356 |
| scholar | rs74315356 |
| rs74315356 | |
| pharmgkb | rs74315356 |
| gwascentral | rs74315356 |
| openSNP | rs74315356 |
| 23andMe | rs74315356 |
| SNPshot | rs74315356 |
| SNPdbe | rs74315356 |
| MSV3d | rs74315356 |
| GWAS Ctlg | rs74315356 |
| Max Magnitude | 8.9 |
c.1311G>A (p.Trp437Ter, W437X or W437*)
Considered "definitely pathogenic" in the Movement Disorder Society Genetic mutation database (MDSGene) for autosomal recessive, early-onset Parkinson disease (type 6)
23andMe calls this i5003752
| ClinVar | |
|---|---|
| Risk | Rs74315356(A;A) |
| Alt | Rs74315356(A;A) |
| Reference | Rs74315356(G;G) |
| Significance | Pathogenic |
| Disease | Parkinson disease 6 |
| Variation | info |
| Gene | PINK1-AS PINK1 |
| CLNDBN | Parkinson disease 6, autosomal recessive early-onset |
| Reversed | 0 |
| HGVS | NC_000001.10:g.20975547G>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000002507.2, |
