{{Rsnum
|rsid=2860580
|Gene=HCG4P5
|Chromosome=6
|position=29938914
|Orientation=minus
|GMAF=0.3802
|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 | 33.6 | 54.0 | 12.4
| HCB | 37.2 | 51.8 | 10.9
| JPT | 85.8 | 13.3 | 0.9
| YRI | 25.9 | 49.7 | 24.5
| ASW | 29.8 | 49.1 | 21.1
| CHB | 37.2 | 51.8 | 10.9
| CHD | 35.2 | 51.9 | 13.0
| GIH | 19.2 | 47.5 | 33.3
| LWK | 33.9 | 49.5 | 16.5
| MEX | 32.8 | 58.6 | 8.6
| MKK | 23.2 | 52.9 | 23.9
| TSI | 35.6 | 52.5 | 11.9
| 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=5E-67
|OR=1.72
|ORtxt=[1.61-1.82]
}}

{{omim
|id=607107
|rsnum=2860580
}}

{{PMID|18519066|OA=1
}} Detection, imputation, and association analysis of small deletions and null alleles on oligonucleotide arrays.

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