rs6710823
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6710823(A;A) |
| Make rs6710823(A;G) |
| Make rs6710823(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 134834811 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6710823 |
| dbSNP (classic) | rs6710823 |
| ClinGen | rs6710823 |
| ebi | rs6710823 |
| HLI | rs6710823 |
| Exac | rs6710823 |
| Gnomad | rs6710823 |
| Varsome | rs6710823 |
| LitVar | rs6710823 |
| Map | rs6710823 |
| PheGenI | rs6710823 |
| Biobank | rs6710823 |
| 1000 genomes | rs6710823 |
| hgdp | rs6710823 |
| ensembl | rs6710823 |
| geneview | rs6710823 |
| scholar | rs6710823 |
| rs6710823 | |
| pharmgkb | rs6710823 |
| gwascentral | rs6710823 |
| openSNP | rs6710823 |
| 23andMe | rs6710823 |
| SNPshot | rs6710823 |
| SNPdbe | rs6710823 |
| MSV3d | rs6710823 |
| GWAS Ctlg | rs6710823 |
| GMAF | 0.1786 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 21292315 ]
|
| Trait | |
| Title | Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies |
| Risk Allele | G |
| P-val | 7E-9 |
| Odds Ratio | 1.1000 [1.06-1.14] |
