rs34372695
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs34372695(C;T) |
| Make rs34372695(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 156060246 |
| Gene | RAB25 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34372695 |
| dbSNP (classic) | rs34372695 |
| ClinGen | rs34372695 |
| ebi | rs34372695 |
| HLI | rs34372695 |
| Exac | rs34372695 |
| Gnomad | rs34372695 |
| Varsome | rs34372695 |
| LitVar | rs34372695 |
| Map | rs34372695 |
| PheGenI | rs34372695 |
| Biobank | rs34372695 |
| 1000 genomes | rs34372695 |
| hgdp | rs34372695 |
| ensembl | rs34372695 |
| geneview | rs34372695 |
| scholar | rs34372695 |
| rs34372695 | |
| pharmgkb | rs34372695 |
| gwascentral | rs34372695 |
| openSNP | rs34372695 |
| 23andMe | rs34372695 |
| SNPshot | rs34372695 |
| SNPdbe | rs34372695 |
| MSV3d | rs34372695 |
| GWAS Ctlg | rs34372695 |
| GMAF | 0.01286 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| 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 | T |
| P-val | 4E-12 |
| Odds Ratio | 1.4700 [1.35-1.59] |
[PMID 22786590] Large-scale replication and heterogeneity in Parkinson disease genetic loci
[PMID 32253955] The rs3129882/rs4248166 in HLA-DRA and rs34372695 in SYT 11 are not associated with sporadic Parkinson's disease in central Chinese population.
