rs2245218
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 |
| Make rs2245218(A;A) |
| Make rs2245218(A;G) |
| Make rs2245218(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 13813331 |
| Gene | PRDM2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2245218 |
| dbSNP (classic) | rs2245218 |
| ClinGen | rs2245218 |
| ebi | rs2245218 |
| HLI | rs2245218 |
| Exac | rs2245218 |
| Gnomad | rs2245218 |
| Varsome | rs2245218 |
| LitVar | rs2245218 |
| Map | rs2245218 |
| PheGenI | rs2245218 |
| Biobank | rs2245218 |
| 1000 genomes | rs2245218 |
| hgdp | rs2245218 |
| ensembl | rs2245218 |
| geneview | rs2245218 |
| scholar | rs2245218 |
| rs2245218 | |
| pharmgkb | rs2245218 |
| gwascentral | rs2245218 |
| openSNP | rs2245218 |
| 23andMe | rs2245218 |
| SNPshot | rs2245218 |
| SNPdbe | rs2245218 |
| MSV3d | rs2245218 |
| GWAS Ctlg | rs2245218 |
| GMAF | 0.1685 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
rs2245218 increases susceptibility to Parkinson's disease 1.67 times for carriers of the G allele [PMID 16252231
]
[PMID 16685661] Genomewide association, Parkinson disease, and PARK10.
[PMID 16685662] No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.
[PMID 16685663] A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.
