{{Rsnum
|rsid=1572072
|Chromosome=13
|position=23553071
|Orientation=plus
|GMAF=0.3214
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 38.9 | 50.4 | 10.6
| HCB | 62.2 | 31.9 | 5.9
| JPT | 53.1 | 38.1 | 8.8
| YRI | 63.9 | 30.6 | 5.4
| ASW | 49.1 | 43.9 | 7.0
| CHB | 62.2 | 31.9 | 5.9
| CHD | 56.9 | 37.6 | 5.5
| GIH | 14.9 | 55.4 | 29.7
| LWK | 53.6 | 36.4 | 10.0
| MEX | 37.9 | 50.0 | 12.1
| MKK | 52.6 | 39.1 | 8.3
| TSI | 38.2 | 49.0 | 12.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20512145
|Trait=Nasopharyngeal carcinoma
|Title=A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci.
|RiskAllele=
|Pval=1E-8
|OR=1.19
|ORtxt=[1.11-1.27]
}}

{{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}}