rs1721082
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1721082(A;A) |
| Make rs1721082(A;T) |
| Make rs1721082(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 16992623 |
| Gene | FGF20 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1721082 |
| dbSNP (classic) | rs1721082 |
| ClinGen | rs1721082 |
| ebi | rs1721082 |
| HLI | rs1721082 |
| Exac | rs1721082 |
| Gnomad | rs1721082 |
| Varsome | rs1721082 |
| LitVar | rs1721082 |
| Map | rs1721082 |
| PheGenI | rs1721082 |
| Biobank | rs1721082 |
| 1000 genomes | rs1721082 |
| hgdp | rs1721082 |
| ensembl | rs1721082 |
| geneview | rs1721082 |
| scholar | rs1721082 |
| rs1721082 | |
| pharmgkb | rs1721082 |
| gwascentral | rs1721082 |
| openSNP | rs1721082 |
| 23andMe | rs1721082 |
| SNPshot | rs1721082 |
| SNPdbe | rs1721082 |
| MSV3d | rs1721082 |
| GWAS Ctlg | rs1721082 |
| GMAF | 0.3737 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
Associated with Parkinson's disease based on a conditional logistic regression analysis.[PMID 18205889]
[PMID 18252210
] Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synuclein.
