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rs1064795117

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome16
Position78432739
GeneWWOX
is asnp
is mentioned by
dbSNPrs1064795117
dbSNP (old)rs1064795117
ClinGenrs1064795117
ebirs1064795117
HLIrs1064795117
Exacrs1064795117
Gnomadrs1064795117
Varsomers1064795117
Maprs1064795117
PheGenIrs1064795117
Biobankrs1064795117
1000 genomesrs1064795117
hgdprs1064795117
ensemblrs1064795117
gopubmedrs1064795117
geneviewrs1064795117
scholarrs1064795117
googlers1064795117
pharmgkbrs1064795117
gwascentralrs1064795117
openSNPrs1064795117
23andMers1064795117
23andMe allrs1064795117
SNPshotrs1064795117
SNPdbers1064795117
MSV3drs1064795117
GWAS Ctlgrs1064795117
Max Magnitude0
ClinVar
Risk rs1064795117(-;-)
Alt rs1064795117(-;-)
Reference Rs1064795117(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WWOX
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.78466636delT
CLNSRC
CLNACC RCV000484968.1,