rs4964469
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4964469(A;A) |
| Make rs4964469(A;G) |
| Make rs4964469(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 106556209 |
| Gene | LOC100287944 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4964469 |
| dbSNP (classic) | rs4964469 |
| ClinGen | rs4964469 |
| ebi | rs4964469 |
| HLI | rs4964469 |
| Exac | rs4964469 |
| Gnomad | rs4964469 |
| Varsome | rs4964469 |
| LitVar | rs4964469 |
| Map | rs4964469 |
| PheGenI | rs4964469 |
| Biobank | rs4964469 |
| 1000 genomes | rs4964469 |
| hgdp | rs4964469 |
| ensembl | rs4964469 |
| geneview | rs4964469 |
| scholar | rs4964469 |
| rs4964469 | |
| pharmgkb | rs4964469 |
| gwascentral | rs4964469 |
| openSNP | rs4964469 |
| 23andMe | rs4964469 |
| SNPshot | rs4964469 |
| SNPdbe | rs4964469 |
| MSV3d | rs4964469 |
| GWAS Ctlg | rs4964469 |
| GMAF | 0.4513 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21084426] |
| Trait | |
| Title | Genome-wide association study confirms BST1 and suggests a locus on 12q24 as risk loci for Parkinson's disease in the European population |
| Risk Allele | A |
| P-val | 2E-7 |
| Odds Ratio | 1.1600 [1.09-1.22] |
