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rs116333061

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs116333061(G;T)
Make rs116333061(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position132329641
GeneSETX
is asnp
is mentioned by
dbSNPrs116333061
ebirs116333061
HLIrs116333061
Exacrs116333061
Varsomers116333061
Maprs116333061
PheGenIrs116333061
hapmaprs116333061
1000 genomesrs116333061
hgdprs116333061
ensemblrs116333061
gopubmedrs116333061
geneviewrs116333061
scholarrs116333061
googlers116333061
pharmgkbrs116333061
gwascentralrs116333061
openSNPrs116333061
23andMers116333061
23andMe allrs116333061
SNP Nexus

SNPshotrs116333061
SNPdbers116333061
MSV3drs116333061
GWAS Ctlgrs116333061
GMAF0.004132
Max Magnitude0
ClinVar
Risk rs116333061(T;T)
Alt rs116333061(T;T)
Reference rs116333061(G;G)
Significance Pathogenic
Disease Spinocerebellar ataxia autosomal recessive 1
Variation info
Gene SETX
CLNDBN Spinocerebellar ataxia autosomal recessive 1
Reversed 0
HGVS NC_000009.11:g.135205028G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002383.3,