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rs878855021

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878855021(C;G)
Make rs878855021(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position78425043
GeneWWOX
is asnp
is mentioned by
dbSNPrs878855021
ebirs878855021
HLIrs878855021
Exacrs878855021
Varsomers878855021
Maprs878855021
PheGenIrs878855021
hapmaprs878855021
1000 genomesrs878855021
hgdprs878855021
ensemblrs878855021
gopubmedrs878855021
geneviewrs878855021
scholarrs878855021
googlers878855021
pharmgkbrs878855021
gwascentralrs878855021
openSNPrs878855021
23andMers878855021
23andMe allrs878855021
SNP Nexus

SNPshotrs878855021
SNPdbers878855021
MSV3drs878855021
GWAS Ctlgrs878855021
Max Magnitude0
ClinVar
Risk rs878855021(G;G)
Alt rs878855021(G;G)
Reference rs878855021(C;C)
Significance Pathogenic
Disease Epileptic encephalopathy Spinocerebellar ataxia
Variation info
Gene WWOX
CLNDBN Epileptic encephalopathy, early infantile, 1 Spinocerebellar ataxia, autosomal recessive 12
Reversed 0
HGVS NC_000016.9:g.78458940C>G
CLNSRC
CLNACC RCV000234306.1,