rs2242330
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2242330(C;C) |
| Make rs2242330(C;T) |
| Make rs2242330(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 67581531 |
| Gene | STAP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2242330 |
| dbSNP (classic) | rs2242330 |
| ClinGen | rs2242330 |
| ebi | rs2242330 |
| HLI | rs2242330 |
| Exac | rs2242330 |
| Gnomad | rs2242330 |
| Varsome | rs2242330 |
| LitVar | rs2242330 |
| Map | rs2242330 |
| PheGenI | rs2242330 |
| Biobank | rs2242330 |
| 1000 genomes | rs2242330 |
| hgdp | rs2242330 |
| ensembl | rs2242330 |
| geneview | rs2242330 |
| scholar | rs2242330 |
| rs2242330 | |
| pharmgkb | rs2242330 |
| gwascentral | rs2242330 |
| openSNP | rs2242330 |
| 23andMe | rs2242330 |
| SNPshot | rs2242330 |
| SNPdbe | rs2242330 |
| MSV3d | rs2242330 |
| GWAS Ctlg | rs2242330 |
| GMAF | 0.2025 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS | |
|---|---|
| SNP | rs2242330 |
| PubMedID | [PMID 17052657] |
| Condition | Parkinson's disease |
| Gene | BRDG1 |
| Risk Allele | |
| pValue | 2.00E-006 |
| OR | 2 |
| 95% CI | 1.43-2.50 |
[PMID 20369022
] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.
