Have questions? Visit https://www.reddit.com/r/SNPedia

rs587777128

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777128(A;A)
Make rs587777128(A;C)
ReferenceGRCh38 38.1/142
Chromosome16
Position78108454
GeneWWOX
is asnp
is mentioned by
dbSNPrs587777128
ebirs587777128
HLIrs587777128
Exacrs587777128
Varsomers587777128
Maprs587777128
PheGenIrs587777128
hapmaprs587777128
1000 genomesrs587777128
hgdprs587777128
ensemblrs587777128
gopubmedrs587777128
geneviewrs587777128
scholarrs587777128
googlers587777128
pharmgkbrs587777128
gwascentralrs587777128
openSNPrs587777128
23andMers587777128
23andMe allrs587777128
SNP Nexus

SNPshotrs587777128
SNPdbers587777128
MSV3drs587777128
GWAS Ctlgrs587777128
Max Magnitude0
ClinVar
Risk rs587777128(A;A)
Alt rs587777128(A;A)
Reference rs587777128(C;C)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene WWOX
CLNDBN Spinocerebellar ataxia, autosomal recessive 12
Reversed 0
HGVS NC_000016.9:g.78142351C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000087049.3,