{{Rsnum
|rsid=1318772
|Gene=MCC
|Chromosome=5
|position=113387870
|Orientation=plus
|GMAF=0.1423
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MCC
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 75.2 | 23.0 | 1.8
| HCB | 94.9 | 5.1 | 0.0
| JPT | 91.2 | 8.8 | 0.0
| YRI | 37.4 | 48.3 | 14.3
| ASW | 52.6 | 35.1 | 12.3
| CHB | 94.9 | 5.1 | 0.0
| CHD | 96.3 | 3.7 | 0.0
| GIH | 86.1 | 13.9 | 0.0
| LWK | 45.5 | 42.7 | 11.8
| MEX | 91.4 | 8.6 | 0.0
| MKK | 59.0 | 35.9 | 5.1
| TSI | 84.3 | 14.7 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21326311
|Trait=None
|Title=Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients
|RiskAllele=G
|Pval=0.000001
|OR=0.9100
|ORtxt=[0.54-1.28] unit decrease
}}

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