{{Rsnum
|rsid=966423
|Gene=DIRC3
|Chromosome=2
|position=217445617
|Orientation=plus
|GMAF=0.3696
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=DIRC3
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 17.7 | 55.8 | 26.5
| HCB | 57.7 | 38.7 | 3.6
| JPT | 46.9 | 45.1 | 8.0
| YRI | 69.4 | 29.3 | 1.4
| ASW | 57.9 | 33.3 | 8.8
| CHB | 57.7 | 38.7 | 3.6
| CHD | 64.2 | 29.4 | 6.4
| GIH | 56.4 | 35.6 | 7.9
| LWK | 79.1 | 18.2 | 2.7
| MEX | 53.4 | 39.7 | 6.9
| MKK | 72.4 | 25.0 | 2.6
| TSI | 19.6 | 43.1 | 37.3
| HapMapRevision=28
}}

{{PMID Auto GWAS
|PMID=22267200
|Trait=None
|Title=Discovery of common variants associated with low TSH levels and thyroid cancer risk.
|RiskAllele=C
|Pval=1E-9
|OR=1.3400
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=19481195
|Title=The primordial growth disorder 3-M syndrome connects ubiquitination to the cytoskeletal adaptor OBSL1.
|OA=1
}}

{{PMID Auto
|PMID=23659773
|Title=Cumulative Risk Impact of Five Genetic Variants Associated With Papillary Thyroid Carcinoma
}}

{{PMID Auto
|PMID=23847140
|Title=Confirmation of papillary thyroid cancer susceptibility loci identified by genome-wide association studies of chromosomes 14q13, 9q22, 2q35 and 8p12 in a Chinese population
}}

{{PMID Auto
|PMID=24591304
|Title=Significant SNPs have limited prediction ability for thyroid cancer
}}
{{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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}