{{Rsnum
|rsid=2288034
|Gene=WWOX
|Chromosome=16
|position=79212059
|Orientation=minus
|GMAF=0.4688
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=WWOX
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 38.5 | 47.7 | 13.8
| HCB | 13.3 | 46.7 | 40.0
| JPT | 18.2 | 47.7 | 34.1
| YRI | 14.5 | 41.9 | 43.5
| ASW | 0.0 | 0.0 | 0.0
| CHB | 13.3 | 46.7 | 40.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=2288034
|allele=G
|frequency=0.684
|uid=1103645525016
|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 = 383362
| distance = 136
}}
{{ neighbor
| rsid = 2288033
| distance = 5
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}