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rs397515475

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TCT;TCT) 0 common in clinvar
Make rs397515475(-;-)
Make rs397515475(-;TCT)
ReferenceGRCh38 38.1/141
Chromosome1
Position111982045
GeneKCND3
is asnp
is mentioned by
dbSNPrs397515475
ebirs397515475
HLIrs397515475
Exacrs397515475
Varsomers397515475
Maprs397515475
PheGenIrs397515475
hapmaprs397515475
1000 genomesrs397515475
hgdprs397515475
ensemblrs397515475
gopubmedrs397515475
geneviewrs397515475
scholarrs397515475
googlers397515475
pharmgkbrs397515475
gwascentralrs397515475
openSNPrs397515475
23andMers397515475
23andMe allrs397515475
SNP Nexus

SNPshotrs397515475
SNPdbers397515475
MSV3drs397515475
GWAS Ctlgrs397515475
Max Magnitude0
ClinVar
Risk rs397515475(;)
Alt rs397515475(;)
Reference rs397515475(TCT;TCT)
Significance Pathogenic
Disease Spinocerebellar ataxia 19
Variation info
Gene KCND3
CLNDBN Spinocerebellar ataxia 19
Reversed 1
HGVS NC_000001.10:g.112524667_112524669delAGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000056298.2,