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rs267606941

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606941(G;T)
Make rs267606941(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position1980674
GenePDYN
is asnp
is mentioned by
dbSNPrs267606941
ebirs267606941
HLIrs267606941
Exacrs267606941
Varsomers267606941
Maprs267606941
PheGenIrs267606941
hapmaprs267606941
1000 genomesrs267606941
hgdprs267606941
ensemblrs267606941
gopubmedrs267606941
geneviewrs267606941
scholarrs267606941
googlers267606941
pharmgkbrs267606941
gwascentralrs267606941
openSNPrs267606941
23andMers267606941
23andMe allrs267606941
SNP Nexus

SNPshotrs267606941
SNPdbers267606941
MSV3drs267606941
GWAS Ctlgrs267606941
Max Magnitude0
ClinVar
Risk rs267606941(T;T)
Alt rs267606941(T;T)
Reference rs267606941(G;G)
Significance Pathogenic
Disease Spinocerebellar ataxia 23
Variation info
Gene PDYN LOC727993
CLNDBN Spinocerebellar ataxia 23
Reversed 1
HGVS NC_000020.10:g.1961320C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018094.27,