rs1721100
| Orientation | minus |
| Stabilized | minus |
| Make rs1721100(C;C) |
| Make rs1721100(C;G) |
| Make rs1721100(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 16992989 |
| Gene | FGF20 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1721100 |
| dbSNP (classic) | rs1721100 |
| ClinGen | rs1721100 |
| ebi | rs1721100 |
| HLI | rs1721100 |
| Exac | rs1721100 |
| Gnomad | rs1721100 |
| Varsome | rs1721100 |
| LitVar | rs1721100 |
| Map | rs1721100 |
| PheGenI | rs1721100 |
| Biobank | rs1721100 |
| 1000 genomes | rs1721100 |
| hgdp | rs1721100 |
| ensembl | rs1721100 |
| geneview | rs1721100 |
| scholar | rs1721100 |
| rs1721100 | |
| pharmgkb | rs1721100 |
| gwascentral | rs1721100 |
| openSNP | rs1721100 |
| 23andMe | rs1721100 |
| SNPshot | rs1721100 |
| SNPdbe | rs1721100 |
| MSV3d | rs1721100 |
| GWAS Ctlg | rs1721100 |
| GMAF | 0.4137 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 18205889] Parkinson's disease The risk alleles for each SNP identified from conditional logistic regression, rs1721100 C, rs1721082 T and rs1799836 A, are consistent with previous reports. Significant interaction between this FGF20 SNP and a MAOB gene SNP, rs1799836 was also noticed.
[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 17515805] Fibroblast growth factor 20 gene and Parkinson's disease in the Japanese population.
[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.
[PMID 22342445] Fibroblast growth factor 20 (FGF20) polymorphism is a risk factor for Parkinson's disease in Chinese population.
[PMID 23938014] Fibroblast growth factor 20 polymorphism in sporadic Parkinson's disease in Northern Han Chinese
[PMID 25030126] Quantitative assessment of the association between fibroblast growth factor 20 rs1721100 C/G polymorphism and the risk of sporadic Parkinson's diseases: a meta-analysis
