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rs587777127

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777127(C;C)
Make rs587777127(C;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position79211665
GeneWWOX
is asnp
is mentioned by
dbSNPrs587777127
ebirs587777127
HLIrs587777127
Exacrs587777127
Varsomers587777127
Maprs587777127
PheGenIrs587777127
hapmaprs587777127
1000 genomesrs587777127
hgdprs587777127
ensemblrs587777127
gopubmedrs587777127
geneviewrs587777127
scholarrs587777127
googlers587777127
pharmgkbrs587777127
gwascentralrs587777127
openSNPrs587777127
23andMers587777127
23andMe allrs587777127
SNP Nexus

SNPshotrs587777127
SNPdbers587777127
MSV3drs587777127
GWAS Ctlgrs587777127
Max Magnitude0
ClinVar
Risk rs587777127(C;C)
Alt rs587777127(C;C)
Reference rs587777127(G;G)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene WWOX
CLNDBN Spinocerebellar ataxia, autosomal recessive 12
Reversed 0
HGVS NC_000016.9:g.79245562G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000087048.3,