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rs121434377

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434377(C;T)
Make rs121434377(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position132328996
GeneSETX
is asnp
is mentioned by
dbSNPrs121434377
ebirs121434377
HLIrs121434377
Exacrs121434377
Varsomers121434377
Maprs121434377
PheGenIrs121434377
hapmaprs121434377
1000 genomesrs121434377
hgdprs121434377
ensemblrs121434377
gopubmedrs121434377
geneviewrs121434377
scholarrs121434377
googlers121434377
pharmgkbrs121434377
gwascentralrs121434377
openSNPrs121434377
23andMers121434377
23andMe allrs121434377
SNP Nexus

SNPshotrs121434377
SNPdbers121434377
MSV3drs121434377
GWAS Ctlgrs121434377
Max Magnitude0
OMIM608465
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121434377(T;T)
Alt rs121434377(T;T)
Reference rs121434377(C;C)
Significance Pathogenic
Disease Spinocerebellar ataxia autosomal recessive 1
Variation info
Gene SETX
CLNDBN Spinocerebellar ataxia autosomal recessive 1
Reversed 1
HGVS NC_000009.11:g.135204383G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002375.3,