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rs1721100

From SNPedia

Orientationminus
Stabilizedminus
Make rs1721100(C;C)
Make rs1721100(C;G)
Make rs1721100(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position16992989
GeneFGF20
is asnp
is mentioned by
dbSNPrs1721100
ebirs1721100
HLIrs1721100
Exacrs1721100
Varsomers1721100
Maprs1721100
PheGenIrs1721100
hapmaprs1721100
1000 genomesrs1721100
hgdprs1721100
ensemblrs1721100
gopubmedrs1721100
geneviewrs1721100
scholarrs1721100
googlers1721100
pharmgkbrs1721100
gwascentralrs1721100
openSNPrs1721100
23andMers1721100
23andMe allrs1721100
SNP Nexus

SNPshotrs1721100
SNPdbers1721100
MSV3drs1721100
GWAS Ctlgrs1721100
GMAF0.4137
Max Magnitude
? (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.

Neighborrs1721082
Distance366
OMIM605558
DescFIBROBLAST GROWTH FACTOR 20; FGF20
Variant
Relatedalso
[PMID 15122513OA-icon.png] Fibroblast growth factor 20 polymorphisms and haplotypes strongly influence risk of Parkinson disease.


[PMID 15967032OA-icon.png] 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 18252210OA-icon.png] Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synuclein.


[PMID 19133659OA-icon.png] 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