{{Rsnum
|rsid=383362
|Gene=WWOX
|Chromosome=16
|position=79211923
|Orientation=plus
|GMAF=0.3508
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=WWOX
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 19.6 | 50.9 | 29.5
| HCB | 77.0 | 21.5 | 1.5
| JPT | 71.4 | 26.8 | 1.8
| YRI | 40.8 | 44.9 | 14.3
| ASW | 42.1 | 42.1 | 15.8
| CHB | 77.0 | 21.5 | 1.5
| CHD | 77.8 | 20.4 | 1.9
| GIH | 32.7 | 52.5 | 14.9
| LWK | 54.6 | 37.0 | 8.3
| MEX | 55.2 | 32.8 | 12.1
| MKK | 57.1 | 33.1 | 9.7
| TSI | 23.5 | 47.1 | 29.4
| HapMapRevision=28
}}{{Venter SNP
|rsid=383362
|allele=T
|frequency=0.583
|uid=1103645525015
|type=homozygous_SNP
|hugo=Q9NZC7-8
|ensembl gene=ENSG00000186153
|ensembl transcript=ENST00000329729
|sift=TOLERATED
|disease=Defects in WWOX may be involved in esophageal squamous cell carcinoma (ESCC) (MIM:133239).
}}

{{ neighbor
| rsid = 2288034
| distance = 136
}}

{{PMID Auto
|PMID=22693020
|Title=The polymorphisms and haplotypes of WWOX gene are associated with the risk of lung cancer in southern and eastern Chinese populations.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}