{{Rsnum
|rsid=12421680
|Gene=NTM
|Chromosome=11
|position=131481074
|Orientation=plus
|GMAF=0.4821
|Gene_s=NTM
|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 | 10.7 | 43.8 | 45.5
| HCB | 51.1 | 39.3 | 9.6
| JPT | 38.9 | 44.2 | 16.8
| YRI | 42.9 | 42.9 | 14.3
| ASW | 24.6 | 57.9 | 17.5
| CHB | 51.1 | 39.3 | 9.6
| CHD | 43.1 | 48.6 | 8.3
| GIH | 8.9 | 51.5 | 39.6
| LWK | 32.7 | 52.7 | 14.5
| MEX | 51.7 | 36.2 | 12.1
| MKK | 33.3 | 50.6 | 16.0
| TSI | 10.8 | 44.1 | 45.1
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23548203
  |Trait=Sunburns
  |Title=Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.
  |RiskAllele=A
  |Pval=6E-6
  |OR=.41
  |ORtxt=[0.23-0.59] unit increase
  }}

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