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rs201486601

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201486601(A;A)
Make rs201486601(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position1980454
GenePDYN
is asnp
is mentioned by
dbSNPrs201486601
ebirs201486601
HLIrs201486601
Exacrs201486601
Varsomers201486601
Maprs201486601
PheGenIrs201486601
hapmaprs201486601
1000 genomesrs201486601
hgdprs201486601
ensemblrs201486601
gopubmedrs201486601
geneviewrs201486601
scholarrs201486601
googlers201486601
pharmgkbrs201486601
gwascentralrs201486601
openSNPrs201486601
23andMers201486601
23andMe allrs201486601
SNP Nexus

SNPshotrs201486601
SNPdbers201486601
MSV3drs201486601
GWAS Ctlgrs201486601
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs201486601(A;A)
Alt rs201486601(A;A)
Reference rs201486601(G;G)
Significance Pathogenic
Disease Spinocerebellar ataxia 23
Variation info
Gene PDYN LOC727993
CLNDBN Spinocerebellar ataxia 23
Reversed 0
HGVS NC_000020.10:g.1961100G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018097.27,