{{Rsnum
|rsid=9929635
|Gene=WWOX
|Chromosome=16
|position=79066662
|Orientation=plus
|GMAF=0.2709
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=WWOX
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 33.9 | 50.9 | 15.2
| HCB | 77.4 | 21.9 | 0.7
| JPT | 68.8 | 29.5 | 1.8
| YRI | 74.0 | 24.0 | 2.1
| ASW | 66.7 | 31.6 | 1.8
| CHB | 77.4 | 21.9 | 0.7
| CHD | 76.1 | 21.1 | 2.8
| GIH | 69.3 | 30.7 | 0.0
| LWK | 69.1 | 27.3 | 3.6
| MEX | 43.1 | 41.4 | 15.5
| MKK | 57.7 | 39.7 | 2.6
| TSI | 42.2 | 46.1 | 11.8
| HapMapRevision=28
}}{{omim
|desc=SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE; SPG35
|id=612319
|rsnum=9929635
}}

{{PMID|18463364}} A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23.

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}