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rs1057517846

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517846(A;A)
Make rs1057517846(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position78108446
GeneWWOX
is asnp
is mentioned by
dbSNPrs1057517846
dbSNP (old)rs1057517846
ClinGenrs1057517846
ebirs1057517846
HLIrs1057517846
Exacrs1057517846
Gnomadrs1057517846
Varsomers1057517846
Maprs1057517846
PheGenIrs1057517846
Biobankrs1057517846
1000 genomesrs1057517846
hgdprs1057517846
ensemblrs1057517846
gopubmedrs1057517846
geneviewrs1057517846
scholarrs1057517846
googlers1057517846
pharmgkbrs1057517846
gwascentralrs1057517846
openSNPrs1057517846
23andMers1057517846
23andMe allrs1057517846
SNPshotrs1057517846
SNPdbers1057517846
MSV3drs1057517846
GWAS Ctlgrs1057517846
Max Magnitude0
ClinVar
Risk rs1057517846(A;A)
Alt rs1057517846(A;A)
Reference Rs1057517846(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene WWOX
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.78142343G>A
CLNSRC
CLNACC RCV000414691.1,