rs6492998
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6492998(A;A) |
| Make rs6492998(A;G) |
| Make rs6492998(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 41254433 |
| Gene | CHP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6492998 |
| dbSNP (classic) | rs6492998 |
| ClinGen | rs6492998 |
| ebi | rs6492998 |
| HLI | rs6492998 |
| Exac | rs6492998 |
| Gnomad | rs6492998 |
| Varsome | rs6492998 |
| LitVar | rs6492998 |
| Map | rs6492998 |
| PheGenI | rs6492998 |
| Biobank | rs6492998 |
| 1000 genomes | rs6492998 |
| hgdp | rs6492998 |
| ensembl | rs6492998 |
| geneview | rs6492998 |
| scholar | rs6492998 |
| rs6492998 | |
| pharmgkb | rs6492998 |
| gwascentral | rs6492998 |
| openSNP | rs6492998 |
| 23andMe | rs6492998 |
| SNPshot | rs6492998 |
| SNPdbe | rs6492998 |
| MSV3d | rs6492998 |
| GWAS Ctlg | rs6492998 |
| GMAF | 0.3012 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21085126] SNPs in axon guidance pathway genes and susceptibility for Parkinson's disease in the Korean population
[PMID 18628988
] Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's disease.
