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rs1721082

From SNPedia

Orientationminus
Stabilizedminus
Make rs1721082(A;A)
Make rs1721082(A;T)
Make rs1721082(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position16992623
GeneFGF20
is asnp
is mentioned by
dbSNPrs1721082
ebirs1721082
HLIrs1721082
Exacrs1721082
Varsomers1721082
Maprs1721082
PheGenIrs1721082
hapmaprs1721082
1000 genomesrs1721082
hgdprs1721082
ensemblrs1721082
gopubmedrs1721082
geneviewrs1721082
scholarrs1721082
googlers1721082
pharmgkbrs1721082
gwascentralrs1721082
openSNPrs1721082
23andMers1721082
23andMe allrs1721082
SNP Nexus

SNPshotrs1721082
SNPdbers1721082
MSV3drs1721082
GWAS Ctlgrs1721082
GMAF0.3737
Max Magnitude
? (A;A) (A;T) (T;T) 28
Associated with Parkinson's disease based on a conditional logistic regression analysis.[PMID 18205889]
Neighborrs1721100
Distance366
[PMID 18252210OA-icon.png] Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synuclein.