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rs1060502727

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502727(C;C)
Make rs1060502727(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position78115155
GeneWWOX
is asnp
is mentioned by
dbSNPrs1060502727
dbSNP (old)rs1060502727
ClinGenrs1060502727
ebirs1060502727
HLIrs1060502727
Exacrs1060502727
Gnomadrs1060502727
Varsomers1060502727
Maprs1060502727
PheGenIrs1060502727
Biobankrs1060502727
1000 genomesrs1060502727
hgdprs1060502727
ensemblrs1060502727
gopubmedrs1060502727
geneviewrs1060502727
scholarrs1060502727
googlers1060502727
pharmgkbrs1060502727
gwascentralrs1060502727
openSNPrs1060502727
23andMers1060502727
23andMe allrs1060502727
SNPshotrs1060502727
SNPdbers1060502727
MSV3drs1060502727
GWAS Ctlgrs1060502727
Max Magnitude0
ClinVar
Risk rs1060502727(C;C)
Alt rs1060502727(C;C)
Reference Rs1060502727(G;G)
Significance Probable-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.78149052G>C
CLNSRC
CLNACC RCV000458905.1,