Rs119487098

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Orientationplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs119487098(C;C)
Make rs119487098(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position78432568
GeneWWOX
is asnp
is mentioned by
dbSNPrs119487098
PheGenIrs119487098
nextbiors119487098
hapmaprs119487098
1000 genomesrs119487098
hgdprs119487098
ensemblrs119487098
gopubmedrs119487098
geneviewrs119487098
scholarrs119487098
googlers119487098
pharmgkbrs119487098
gwascentralrs119487098
openSNPrs119487098
23andMers119487098
23andMe allrs119487098
SNP Nexus

SNPshotrs119487098
SNPdbers119487098
MSV3drs119487098
Max Magnitude0
OMIM605131
Desc
Variant0001
Relatedalso
ClinVar
Risk rs119487098(C;C)
Alt rs119487098(C;C)
Reference rs119487098(T;T)
Significance Other
Disease Esophageal squamous cell carcinoma
Variation info
Gene WWOX
CLNDBN Esophageal squamous cell carcinoma, somatic
Reversed 0
HGVS NC_000016.9:g.78466465T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000005513.1,