rs1989754
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1989754(C;C) |
| Make rs1989754(C;G) |
| Make rs1989754(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 17000966 |
| Gene | FGF20 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1989754 |
| dbSNP (classic) | rs1989754 |
| ClinGen | rs1989754 |
| ebi | rs1989754 |
| HLI | rs1989754 |
| Exac | rs1989754 |
| Gnomad | rs1989754 |
| Varsome | rs1989754 |
| LitVar | rs1989754 |
| Map | rs1989754 |
| PheGenI | rs1989754 |
| Biobank | rs1989754 |
| 1000 genomes | rs1989754 |
| hgdp | rs1989754 |
| ensembl | rs1989754 |
| geneview | rs1989754 |
| scholar | rs1989754 |
| rs1989754 | |
| pharmgkb | rs1989754 |
| gwascentral | rs1989754 |
| openSNP | rs1989754 |
| 23andMe | rs1989754 |
| SNPshot | rs1989754 |
| SNPdbe | rs1989754 |
| MSV3d | rs1989754 |
| GWAS Ctlg | rs1989754 |
| GMAF | 0.405 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 15122513
] Fibroblast growth factor 20 polymorphisms and haplotypes strongly influence risk of Parkinson disease.
[PMID 15967032] Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients.
[PMID 18252210] Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synuclein.
[PMID 19133659] FGF20 and Parkinson's disease: no evidence of association or pathogenicity via alpha-synuclein expression.
