rs17468382
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs17468382(C;C) |
| Make rs17468382(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 52734641 |
| Gene | DCC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17468382 |
| dbSNP (classic) | rs17468382 |
| ClinGen | rs17468382 |
| ebi | rs17468382 |
| HLI | rs17468382 |
| Exac | rs17468382 |
| Gnomad | rs17468382 |
| Varsome | rs17468382 |
| LitVar | rs17468382 |
| Map | rs17468382 |
| PheGenI | rs17468382 |
| Biobank | rs17468382 |
| 1000 genomes | rs17468382 |
| hgdp | rs17468382 |
| ensembl | rs17468382 |
| geneview | rs17468382 |
| scholar | rs17468382 |
| rs17468382 | |
| pharmgkb | rs17468382 |
| gwascentral | rs17468382 |
| openSNP | rs17468382 |
| 23andMe | rs17468382 |
| SNPshot | rs17468382 |
| SNPdbe | rs17468382 |
| MSV3d | rs17468382 |
| GWAS Ctlg | rs17468382 |
| GMAF | 0.02663 |
| Max Magnitude | 0 |
[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.
