{{Rsnum
|rsid=2288033
|Gene=WWOX
|Chromosome=16
|position=79212064
|Orientation=minus
|GMAF=0.4702
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=WWOX
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 15.0 | 44.2 | 40.7
| HCB | 40.1 | 48.2 | 11.7
| JPT | 32.7 | 52.2 | 15.0
| YRI | 23.8 | 53.1 | 23.1
| ASW | 40.4 | 29.8 | 29.8
| CHB | 40.1 | 48.2 | 11.7
| CHD | 48.6 | 34.9 | 16.5
| GIH | 29.7 | 54.5 | 15.8
| LWK | 44.5 | 42.7 | 12.7
| MEX | 44.8 | 39.7 | 15.5
| MKK | 50.6 | 34.0 | 15.4
| TSI | 14.7 | 52.0 | 33.3
| HapMapRevision=28
}}{{Venter SNP
|rsid=2288033
|allele=C
|frequency=0.673
|uid=1103645525017
|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 = 5
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}