{{Rsnum
|rsid=11556924
|Gene=ZC3HC1
|Chromosome=7
|position=130023656
|Orientation=plus
|GMAF=0.1919
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=ZC3HC1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 34.5 | 54.0 | 11.5
| HCB | 91.9 | 8.1 | 0.0
| JPT | 94.7 | 5.3 | 0.0
| YRI | 97.3 | 2.7 | 0.0
| ASW | 78.9 | 19.3 | 1.8
| CHB | 91.9 | 8.1 | 0.0
| CHD | 92.7 | 7.3 | 0.0
| GIH | 71.3 | 26.7 | 2.0
| LWK | 96.3 | 3.7 | 0.0
| MEX | 68.4 | 29.8 | 1.8
| MKK | 92.3 | 7.7 | 0.0
| TSI | 36.3 | 49.0 | 14.7
| HapMapRevision=28
}}
[[Coronary Heart Disease]]

{{PMID Auto
|PMID=24286297
|Title=The ZC3HC1 rs11556924 polymorphism is associated with increased carotid intima-media thickness in patients with rheumatoid arthritis
|OA=1
}}

{{PMID Auto GWAS
  |PMID=24262325
  |Trait=Coronary artery disease
  |Title=Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
  |RiskAllele=T
  |Pval=3E-10
  |OR=1.10
  |ORtxt=[1.06-1.12]
  }}
{{PMID Auto GWAS
|PMID=21378990
|Trait=Coronary artery disease
|Title=Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
|RiskAllele=C
|Pval=9E-18
|OR=1.0900
|ORtxt=[1.07-1.12]
|OA=1
}}

{{GET Evidence
|gene=ZC3HC1
|aa_change=Arg363His
|aa_change_short=R363H
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs11556924
|overall_frequency_n=3018
|overall_frequency_d=10758
|overall_frequency=0.280535
|n_genomes=18
|n_genomes_annotated=0
|n_haplomes=21
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.999
|nblosum100=1
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}