rs12720208
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs12720208(C;T) |
| Make rs12720208(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 8 |
| Position | 16992890 |
| Gene | FGF20 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12720208 |
| dbSNP (classic) | rs12720208 |
| ClinGen | rs12720208 |
| ebi | rs12720208 |
| HLI | rs12720208 |
| Exac | rs12720208 |
| Gnomad | rs12720208 |
| Varsome | rs12720208 |
| LitVar | rs12720208 |
| Map | rs12720208 |
| PheGenI | rs12720208 |
| Biobank | rs12720208 |
| 1000 genomes | rs12720208 |
| hgdp | rs12720208 |
| ensembl | rs12720208 |
| geneview | rs12720208 |
| scholar | rs12720208 |
| rs12720208 | |
| pharmgkb | rs12720208 |
| gwascentral | rs12720208 |
| openSNP | rs12720208 |
| 23andMe | rs12720208 |
| SNPshot | rs12720208 |
| SNPdbe | rs12720208 |
| MSV3d | rs12720208 |
| GWAS Ctlg | rs12720208 |
| GMAF | 0.03214 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20471450] FGF20 rs12720208 SNP and microRNA-433 variation: no association with Parkinson's disease in Spanish patients
[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.
[PMID 19290790] MicroRNA polymorphisms: the future of pharmacogenomics, molecular epidemiology and individualized medicine.
[PMID 20427658] Genetic variation in FGF20 modulates hippocampal biology.
[PMID 20428464] MicroRNA polymorphisms: a giant leap towards personalized medicine.
[PMID 22342445] Fibroblast growth factor 20 (FGF20) polymorphism is a risk factor for Parkinson's disease in Chinese population.
[PMID 23516905] [Analysis of the rs12720208 single-nucleotide polymorphism of the FGF20 gene in Russian patients with sporadic Parkinson's disease]
[PMID 23938014] Fibroblast growth factor 20 polymorphism in sporadic Parkinson's disease in Northern Han Chinese
[PMID 26070653] Variation in the miRNA-433 binding site of FGF20 is a risk factor for Parkinson's disease in Iranian population
| ClinVar | |
|---|---|
| Risk | rs12720208(T;T) |
| Alt | rs12720208(T;T) |
| Reference | Rs12720208(C;C) |
| Significance | Unknown |
| Disease | Parkinson disease |
| Variation | info |
| Gene | FGF20 |
| CLNDBN | Parkinson disease, late-onset |
| Reversed | 1 |
| HGVS | NC_000008.10:g.16850399G>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000005162.2, |
