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rs875989881

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs875989881(C;C)
Make rs875989881(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position66715235
GeneSPTBN2
is asnp
is mentioned by
dbSNPrs875989881
ebirs875989881
HLIrs875989881
Exacrs875989881
Varsomers875989881
Maprs875989881
PheGenIrs875989881
hapmaprs875989881
1000 genomesrs875989881
hgdprs875989881
ensemblrs875989881
gopubmedrs875989881
geneviewrs875989881
scholarrs875989881
googlers875989881
pharmgkbrs875989881
gwascentralrs875989881
openSNPrs875989881
23andMers875989881
23andMe allrs875989881
SNP Nexus

SNPshotrs875989881
SNPdbers875989881
MSV3drs875989881
GWAS Ctlgrs875989881
Max Magnitude0
ClinVar
Risk rs875989881(C;C)
Alt rs875989881(C;C)
Reference rs875989881(T;T)
Significance Probable-Pathogenic
Disease Spinocerebellar ataxia 5
Variation info
Gene SPTBN2
CLNDBN Spinocerebellar ataxia 5
Reversed 1
HGVS NC_000011.9:g.66482706A>G
CLNSRC University Hospital of Geneva
CLNACC RCV000211499.1,