rs806606
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) |
| Make rs806606(C;T) |
| Make rs806606(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 85974061 |
| Gene | LOC101928842 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs806606 |
| dbSNP (classic) | rs806606 |
| ClinGen | rs806606 |
| ebi | rs806606 |
| HLI | rs806606 |
| Exac | rs806606 |
| Gnomad | rs806606 |
| Varsome | rs806606 |
| LitVar | rs806606 |
| Map | rs806606 |
| PheGenI | rs806606 |
| Biobank | rs806606 |
| 1000 genomes | rs806606 |
| hgdp | rs806606 |
| ensembl | rs806606 |
| geneview | rs806606 |
| scholar | rs806606 |
| rs806606 | |
| pharmgkb | rs806606 |
| gwascentral | rs806606 |
| openSNP | rs806606 |
| 23andMe | rs806606 |
| SNPshot | rs806606 |
| SNPdbe | rs806606 |
| MSV3d | rs806606 |
| GWAS Ctlg | rs806606 |
| GMAF | 0.1579 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 17052657] Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.
