{{Rsnum
|rsid=1126179
|Chromosome=16
|position=65861461
|Orientation=minus
|GMAF=0.3641
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LOC101927676
|Gene_s=LOC101927676
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 25.7 | 56.6 | 17.7
| HCB | 63.5 | 33.6 | 2.9
| JPT | 79.6 | 17.7 | 2.7
| YRI | 19.0 | 50.3 | 30.6
| ASW | 15.8 | 38.6 | 45.6
| CHB | 63.5 | 33.6 | 2.9
| CHD | 63.3 | 33.0 | 3.7
| GIH | 46.5 | 45.5 | 7.9
| LWK | 18.2 | 53.6 | 28.2
| MEX | 44.8 | 48.3 | 6.9
| MKK | 24.4 | 52.6 | 23.1
| TSI | 41.2 | 35.3 | 23.5
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23918034
  |Trait=Molar-incisor hypomineralization
  |Title=Genome-wide association study (GWAS) for molar-incisor hypomineralization (MIH).
  |RiskAllele=G
  |Pval=3E-6
  |OR=2.13
  |ORtxt=[1.55-2.92]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}