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rs1989754

From SNPedia

Orientationplus
Stabilizedplus
Make rs1989754(C;C)
Make rs1989754(C;G)
Make rs1989754(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position17000966
GeneFGF20
is asnp
is mentioned by
dbSNPrs1989754
ebirs1989754
HLIrs1989754
Exacrs1989754
Varsomers1989754
Maprs1989754
PheGenIrs1989754
hapmaprs1989754
1000 genomesrs1989754
hgdprs1989754
ensemblrs1989754
gopubmedrs1989754
geneviewrs1989754
scholarrs1989754
googlers1989754
pharmgkbrs1989754
gwascentralrs1989754
openSNPrs1989754
23andMers1989754
23andMe allrs1989754
SNP Nexus

SNPshotrs1989754
SNPdbers1989754
MSV3drs1989754
GWAS Ctlgrs1989754
GMAF0.405
Max Magnitude
? (C;C) (C;G) (G;G) 28
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 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.