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rs794726681

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794726681(-;-)
Make rs794726681(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position43555342
GeneANO10
is asnp
is mentioned by
dbSNPrs794726681
ebirs794726681
HLIrs794726681
Exacrs794726681
Varsomers794726681
Maprs794726681
PheGenIrs794726681
hapmaprs794726681
1000 genomesrs794726681
hgdprs794726681
ensemblrs794726681
gopubmedrs794726681
geneviewrs794726681
scholarrs794726681
googlers794726681
pharmgkbrs794726681
gwascentralrs794726681
openSNPrs794726681
23andMers794726681
23andMe allrs794726681
SNP Nexus

SNPshotrs794726681
SNPdbers794726681
MSV3drs794726681
GWAS Ctlgrs794726681
Max Magnitude0
ClinVar
Risk rs794726681(;)
Alt rs794726681(;)
Reference rs794726681(T;T)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene ANO10
CLNDBN Spinocerebellar ataxia, autosomal recessive 10
Reversed 1
HGVS NC_000003.11:g.43596834delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000024054.4,