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rs794726680

From SNPedia

Orientationminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs794726680(-;-)
Make rs794726680(-;TT)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position43576703
GeneANO10
is asnp
is mentioned by
dbSNPrs794726680
ebirs794726680
HLIrs794726680
Exacrs794726680
Varsomers794726680
Maprs794726680
PheGenIrs794726680
hapmaprs794726680
1000 genomesrs794726680
hgdprs794726680
ensemblrs794726680
gopubmedrs794726680
geneviewrs794726680
scholarrs794726680
googlers794726680
pharmgkbrs794726680
gwascentralrs794726680
openSNPrs794726680
23andMers794726680
23andMe allrs794726680
SNP Nexus

SNPshotrs794726680
SNPdbers794726680
MSV3drs794726680
GWAS Ctlgrs794726680
Max Magnitude0
ClinVar
Risk rs794726680(;)
Alt rs794726680(;)
Reference rs794726680(TT;TT)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene ANO10
CLNDBN Spinocerebellar ataxia, autosomal recessive 10
Reversed 1
HGVS NC_000003.11:g.43618195_43618196delAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000024052.5,