{{Rsnum
|rsid=745080
|Gene=TXNDC16
|Chromosome=14
|position=52522510
|Orientation=minus
|GMAF=0.3871
|Gene_s=TXNDC16
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 49.6 | 35.4 | 15.0
| HCB | 17.5 | 65.0 | 17.5
| JPT | 26.5 | 46.9 | 26.5
| YRI | 45.6 | 42.9 | 11.6
| ASW | 36.8 | 36.8 | 26.3
| CHB | 17.5 | 65.0 | 17.5
| CHD | 21.1 | 49.5 | 29.4
| GIH | 13.9 | 51.5 | 34.7
| LWK | 40.0 | 46.4 | 13.6
| MEX | 50.0 | 37.9 | 12.1
| MKK | 30.8 | 53.8 | 15.4
| TSI | 46.1 | 45.1 | 8.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22419666
|Trait=None
|Title=Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts.
|RiskAllele=
|Pval=8E-7
|OR=1.5900
|ORtxt=None
|OA=1
}}

{{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}}
{{on chip | NatGeo2}}