{{Rsnum
|rsid=11897432
|Gene=THADA
|Chromosome=2
|position=43590366
|Orientation=plus
|GMAF=0.1428
|Gene_s=THADA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 3.5 | 41.6 | 54.9
| HCB | 0.0 | 10.2 | 89.8
| JPT | 0.0 | 9.7 | 90.3
| YRI | 2.1 | 18.6 | 79.3
| ASW | 1.8 | 24.6 | 73.7
| CHB | 0.0 | 10.2 | 89.8
| CHD | 0.0 | 7.5 | 92.5
| GIH | 3.0 | 34.0 | 63.0
| LWK | 0.9 | 27.3 | 71.8
| MEX | 0.0 | 13.8 | 86.2
| MKK | 6.5 | 20.8 | 72.7
| TSI | 2.0 | 38.2 | 59.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23725790
  |Trait=DNA methylation (variation)
  |Title=GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.
  |RiskAllele=A
  |Pval=8E-7
  |OR=NR
  |ORtxt=NR
  }}

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