{{Rsnum
|rsid=9864370
|Gene=MECOM
|Chromosome=3
|position=169198452
|Orientation=plus
|GMAF=0.07438
|Gene_s=MECOM
|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 | 0.9 | 13.3 | 85.8
| HCB | 0.7 | 21.2 | 78.1
| JPT | 0.0 | 16.8 | 83.2
| YRI | 0.0 | 15.0 | 85.0
| ASW | 0.0 | 12.3 | 87.7
| CHB | 0.7 | 21.2 | 78.1
| CHD | 0.9 | 17.4 | 81.7
| GIH | 6.9 | 38.6 | 54.5
| LWK | 1.8 | 11.8 | 86.4
| MEX | 1.7 | 8.6 | 89.7
| MKK | 0.0 | 12.2 | 87.8
| TSI | 0.0 | 6.9 | 93.1
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23502783
  |Trait=Multiple myeloma (hyperdiploidy)
  |Title=The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
  |RiskAllele=G
  |Pval=9E-6
  |OR=2.04
  |ORtxt=[1.49-2.80]
  }}

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