{{Rsnum
|rsid=3129055
|Chromosome=6
|position=29702484
|Orientation=minus
|GMAF=0.2759
|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 | 8.0 | 40.7 | 51.3
| HCB | 13.1 | 46.7 | 40.1
| JPT | 15.9 | 53.1 | 31.0
| YRI | 8.8 | 37.4 | 53.7
| ASW | 3.5 | 31.6 | 64.9
| CHB | 13.1 | 46.7 | 40.1
| CHD | 11.9 | 45.9 | 42.2
| GIH | 11.9 | 57.4 | 30.7
| LWK | 3.6 | 21.8 | 74.5
| MEX | 10.3 | 34.5 | 55.2
| MKK | 7.7 | 34.6 | 57.7
| TSI | 3.9 | 36.3 | 59.8
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19664746
|Trait=Nasopharyngeal Carcinoma
|Title=Genome-wide Association Study Reveals Multiple Nasopharyngeal Carcinoma-Associated Loci within the HLA Region at Chromosome 6p21.
|RiskAllele=G
|Pval=7E-11
|OR=1.51
|ORtxt=[1.34-1.71]
|OA=1
}}

{{omim
|id=161550
|rsnum=3129055
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs3129055
|overall_frequency_n=37
|overall_frequency_d=128
|overall_frequency=0.289062
|n_genomes=24
|n_genomes_annotated=0
|n_haplomes=31
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=2
|webscore=N
}}

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