{{Rsnum
|rsid=13375391
|Gene=HMCN1
|Chromosome=1
|position=185825751
|Orientation=plus
|GMAF=0.01699
|Gene_s=HMCN1
|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 | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 2.2 | 97.8
| JPT | 0.0 | 1.8 | 98.2
| YRI | 0.0 | 10.3 | 89.7
| ASW | 0.0 | 10.5 | 89.5
| CHB | 0.0 | 2.2 | 97.8
| CHD | 0.0 | 2.8 | 97.2
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.9 | 13.6 | 85.5
| MEX | 0.0 | 8.6 | 91.4
| MKK | 0.0 | 3.2 | 96.8
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23534349
  |Trait=QRS duration
  |Title=Generalization of Variants Identified by Genome-Wide Association Studies for Electrocardiographic Traits in African Americans.
  |RiskAllele=A
  |Pval=9E-6
  |OR=5.82
  |ORtxt=[NR] ms increase
  }}

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