rs4130047
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4130047(C;C) |
| Make rs4130047(C;T) |
| Make rs4130047(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 43098270 |
| Gene | RIT2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4130047 |
| dbSNP (classic) | rs4130047 |
| ClinGen | rs4130047 |
| ebi | rs4130047 |
| HLI | rs4130047 |
| Exac | rs4130047 |
| Gnomad | rs4130047 |
| Varsome | rs4130047 |
| LitVar | rs4130047 |
| Map | rs4130047 |
| PheGenI | rs4130047 |
| Biobank | rs4130047 |
| 1000 genomes | rs4130047 |
| hgdp | rs4130047 |
| ensembl | rs4130047 |
| geneview | rs4130047 |
| scholar | rs4130047 |
| rs4130047 | |
| pharmgkb | rs4130047 |
| gwascentral | rs4130047 |
| openSNP | rs4130047 |
| 23andMe | rs4130047 |
| SNPshot | rs4130047 |
| SNPdbe | rs4130047 |
| MSV3d | rs4130047 |
| GWAS Ctlg | rs4130047 |
| GMAF | 0.3301 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21738487 ]
|
| Trait | |
| Title | Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease. |
| Risk Allele | C |
| P-val | 2E-7 |
| Odds Ratio | 1.1600 [1.10-1.23] |
[PMID 28190241] Ras-like without CAAX 2 (RIT2): a susceptibility gene for autism spectrum disorder.
