rs12185268
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common on affy axiom data |
| Make rs12185268(A;G) |
| Make rs12185268(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 45846317 |
| Gene | MAPT-AS1, SPPL2C |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12185268 |
| dbSNP (classic) | rs12185268 |
| ClinGen | rs12185268 |
| ebi | rs12185268 |
| HLI | rs12185268 |
| Exac | rs12185268 |
| Gnomad | rs12185268 |
| Varsome | rs12185268 |
| LitVar | rs12185268 |
| Map | rs12185268 |
| PheGenI | rs12185268 |
| Biobank | rs12185268 |
| 1000 genomes | rs12185268 |
| hgdp | rs12185268 |
| ensembl | rs12185268 |
| geneview | rs12185268 |
| scholar | rs12185268 |
| rs12185268 | |
| pharmgkb | rs12185268 |
| gwascentral | rs12185268 |
| openSNP | rs12185268 |
| 23andMe | rs12185268 |
| SNPshot | rs12185268 |
| SNPdbe | rs12185268 |
| MSV3d | rs12185268 |
| GWAS Ctlg | rs12185268 |
| GMAF | 0.1162 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | A |
| P-val | 3E-14 |
| Odds Ratio | 1.3000 [1.22-1.39] |
[PMID 18985386] Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
[PMID 20070850] Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.
[PMID 25929833] Parkinson's Disease Genetic Loci in Rapid Eye Movement Sleep Behavior Disorder
