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rs1057518795

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518795(-;-)
Make rs1057518795(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position78432614
GeneWWOX
is asnp
is mentioned by
dbSNPrs1057518795
dbSNP (old)rs1057518795
ClinGenrs1057518795
ebirs1057518795
HLIrs1057518795
Exacrs1057518795
Gnomadrs1057518795
Varsomers1057518795
Maprs1057518795
PheGenIrs1057518795
Biobankrs1057518795
1000 genomesrs1057518795
hgdprs1057518795
ensemblrs1057518795
gopubmedrs1057518795
geneviewrs1057518795
scholarrs1057518795
googlers1057518795
pharmgkbrs1057518795
gwascentralrs1057518795
openSNPrs1057518795
23andMers1057518795
23andMe allrs1057518795
SNPshotrs1057518795
SNPdbers1057518795
MSV3drs1057518795
GWAS Ctlgrs1057518795
Max Magnitude0
ClinVar
Risk rs1057518795(-;-)
Alt rs1057518795(-;-)
Reference Rs1057518795(G;G)
Significance Probable-Pathogenic
Disease Epileptic encephalopathy
Variation info
Gene WWOX
CLNDBN Epileptic encephalopathy
Reversed 0
HGVS NC_000016.9:g.78466511delG
CLNSRC
CLNACC RCV000415161.1,