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rs267606940

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606940(C;C)
Make rs267606940(C;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position1980456
GenePDYN
is asnp
is mentioned by
dbSNPrs267606940
ebirs267606940
HLIrs267606940
Exacrs267606940
Varsomers267606940
Maprs267606940
PheGenIrs267606940
hapmaprs267606940
1000 genomesrs267606940
hgdprs267606940
ensemblrs267606940
gopubmedrs267606940
geneviewrs267606940
scholarrs267606940
googlers267606940
pharmgkbrs267606940
gwascentralrs267606940
openSNPrs267606940
23andMers267606940
23andMe allrs267606940
SNP Nexus

SNPshotrs267606940
SNPdbers267606940
MSV3drs267606940
GWAS Ctlgrs267606940
Max Magnitude0
ClinVar
Risk rs267606940(C;C)
Alt rs267606940(C;C)
Reference rs267606940(T;T)
Significance Pathogenic
Disease Spinocerebellar ataxia 23
Variation info
Gene PDYN LOC727993
CLNDBN Spinocerebellar ataxia 23
Reversed 1
HGVS NC_000020.10:g.1961102A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000018096.23,