rs2030737
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2030737(A;A) |
| Make rs2030737(A;G) |
| Make rs2030737(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 135090535 |
| Gene | EPHB1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2030737 |
| dbSNP (classic) | rs2030737 |
| ClinGen | rs2030737 |
| ebi | rs2030737 |
| HLI | rs2030737 |
| Exac | rs2030737 |
| Gnomad | rs2030737 |
| Varsome | rs2030737 |
| LitVar | rs2030737 |
| Map | rs2030737 |
| PheGenI | rs2030737 |
| Biobank | rs2030737 |
| 1000 genomes | rs2030737 |
| hgdp | rs2030737 |
| ensembl | rs2030737 |
| geneview | rs2030737 |
| scholar | rs2030737 |
| rs2030737 | |
| pharmgkb | rs2030737 |
| gwascentral | rs2030737 |
| openSNP | rs2030737 |
| 23andMe | rs2030737 |
| SNPshot | rs2030737 |
| SNPdbe | rs2030737 |
| MSV3d | rs2030737 |
| GWAS Ctlg | rs2030737 |
| GMAF | 0.3747 |
| 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.
