rs6963573
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 |
| Make rs6963573(A;A) |
| Make rs6963573(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 36788795 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6963573 |
| dbSNP (classic) | rs6963573 |
| ClinGen | rs6963573 |
| ebi | rs6963573 |
| HLI | rs6963573 |
| Exac | rs6963573 |
| Gnomad | rs6963573 |
| Varsome | rs6963573 |
| LitVar | rs6963573 |
| Map | rs6963573 |
| PheGenI | rs6963573 |
| Biobank | rs6963573 |
| 1000 genomes | rs6963573 |
| hgdp | rs6963573 |
| ensembl | rs6963573 |
| geneview | rs6963573 |
| scholar | rs6963573 |
| rs6963573 | |
| pharmgkb | rs6963573 |
| gwascentral | rs6963573 |
| openSNP | rs6963573 |
| 23andMe | rs6963573 |
| SNPshot | rs6963573 |
| SNPdbe | rs6963573 |
| MSV3d | rs6963573 |
| GWAS Ctlg | rs6963573 |
| GMAF | 0.07713 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| Rs6963573 | |
|---|---|
| PubMed | [PMID 16252231 ]
|
| Affy Probeset | SNP_A-2183433 |
| Affy Orientation | reverse |
| On GW 5.0 | |
| Alleles A/B | C/T |
| Ancestral | G |
| Population | |
| Allele | A |
| Case Freq. | |
| Control Freq. | |
| Odds Ratio Het | |
| Odds Ratio Hom | |
| Odds Ratio All | 1.71 |
| Disease | Parkinson's disease (PKD) |
rs6963573 is in linkage disequilibrium with a polymorphism that increases susceptibility to Parkinson's disease 1.71 times for carriers of the A allele [PMID 16252231]
