rs6599388
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6599388(C;C) |
| Make rs6599388(C;T) |
| Make rs6599388(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 945299 |
| Gene | TMEM175 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6599388 |
| dbSNP (classic) | rs6599388 |
| ClinGen | rs6599388 |
| ebi | rs6599388 |
| HLI | rs6599388 |
| Exac | rs6599388 |
| Gnomad | rs6599388 |
| Varsome | rs6599388 |
| LitVar | rs6599388 |
| Map | rs6599388 |
| PheGenI | rs6599388 |
| Biobank | rs6599388 |
| 1000 genomes | rs6599388 |
| hgdp | rs6599388 |
| ensembl | rs6599388 |
| geneview | rs6599388 |
| scholar | rs6599388 |
| rs6599388 | |
| pharmgkb | rs6599388 |
| gwascentral | rs6599388 |
| openSNP | rs6599388 |
| 23andMe | rs6599388 |
| SNPshot | rs6599388 |
| SNPdbe | rs6599388 |
| MSV3d | rs6599388 |
| GWAS Ctlg | rs6599388 |
| GMAF | 0.3044 |
| 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 | T |
| P-val | 4E-12 |
| Odds Ratio | 1.1600 [1.12-1.20] |
[PMID 26535683] Screening of polymorphisms located in the FGF20 and TMEM175 genes in North Chinese Parkinson's disease patients
