rs4302647
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs4302647(A;A) |
| Make rs4302647(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 94056539 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4302647 |
| dbSNP (classic) | rs4302647 |
| ClinGen | rs4302647 |
| ebi | rs4302647 |
| HLI | rs4302647 |
| Exac | rs4302647 |
| Gnomad | rs4302647 |
| Varsome | rs4302647 |
| LitVar | rs4302647 |
| Map | rs4302647 |
| PheGenI | rs4302647 |
| Biobank | rs4302647 |
| 1000 genomes | rs4302647 |
| hgdp | rs4302647 |
| ensembl | rs4302647 |
| geneview | rs4302647 |
| scholar | rs4302647 |
| rs4302647 | |
| pharmgkb | rs4302647 |
| gwascentral | rs4302647 |
| openSNP | rs4302647 |
| 23andMe | rs4302647 |
| SNPshot | rs4302647 |
| SNPdbe | rs4302647 |
| MSV3d | rs4302647 |
| GWAS Ctlg | rs4302647 |
| GMAF | 0.08494 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21488853
] A genome-wide linkage screen in the Amish with Parkinson disease points to chromosome 6
