{{Rsnum
|rsid=13058467
|Gene=TTLL12
|Chromosome=22
|position=43183043
|Orientation=plus
|GMAF=0.06061
|Gene_s=TTLL12
|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 | 1.8 | 19.5 | 78.8
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.7 | 11.1 | 88.2
| ASW | 0.0 | 12.3 | 87.7
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 5.9 | 94.1
| LWK | 0.0 | 11.0 | 89.0
| MEX | 0.0 | 10.5 | 89.5
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 15.0 | 85.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23918034
  |Trait=Molar-incisor hypomineralization
  |Title=Genome-wide association study (GWAS) for molar-incisor hypomineralization (MIH).
  |RiskAllele=C
  |Pval=4E-7
  |OR=4.40
  |ORtxt=[2.5-7.8]
  }}

{{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}}