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rs387907089

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387907089(G;G)
Make rs387907089(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position43555417
GeneANO10
is asnp
is mentioned by
dbSNPrs387907089
ebirs387907089
HLIrs387907089
Exacrs387907089
Varsomers387907089
Maprs387907089
PheGenIrs387907089
hapmaprs387907089
1000 genomesrs387907089
hgdprs387907089
ensemblrs387907089
gopubmedrs387907089
geneviewrs387907089
scholarrs387907089
googlers387907089
pharmgkbrs387907089
gwascentralrs387907089
openSNPrs387907089
23andMers387907089
23andMe allrs387907089
SNP Nexus

SNPshotrs387907089
SNPdbers387907089
MSV3drs387907089
GWAS Ctlgrs387907089
Max Magnitude0
ClinVar
Risk rs387907089(G;G)
Alt rs387907089(G;G)
Reference rs387907089(T;T)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene ANO10
CLNDBN Spinocerebellar ataxia, autosomal recessive 10
Reversed 1
HGVS NC_000003.11:g.43596909A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000024051.2,