rs4837628
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4837628(C;C) |
| Make rs4837628(C;T) |
| Make rs4837628(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 119297431 |
| Gene | BRINP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4837628 |
| dbSNP (classic) | rs4837628 |
| ClinGen | rs4837628 |
| ebi | rs4837628 |
| HLI | rs4837628 |
| Exac | rs4837628 |
| Gnomad | rs4837628 |
| Varsome | rs4837628 |
| LitVar | rs4837628 |
| Map | rs4837628 |
| PheGenI | rs4837628 |
| Biobank | rs4837628 |
| 1000 genomes | rs4837628 |
| hgdp | rs4837628 |
| ensembl | rs4837628 |
| geneview | rs4837628 |
| scholar | rs4837628 |
| rs4837628 | |
| pharmgkb | rs4837628 |
| gwascentral | rs4837628 |
| openSNP | rs4837628 |
| 23andMe | rs4837628 |
| SNPshot | rs4837628 |
| SNPdbe | rs4837628 |
| MSV3d | rs4837628 |
| GWAS Ctlg | rs4837628 |
| GMAF | 0.4412 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20070850 ]
|
| Trait | Parkinson's disease |
| Title | Genome-Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease |
| Risk Allele | A |
| P-val | 0.000001 |
| Odds Ratio | 1.27 [1.15-1.39] |
