{{Rsnum
|rsid=2302777
|Gene=MED24
|Chromosome=17
|position=40023239
|Orientation=plus
|GMAF=0.3159
|Gene_s=MED24
|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 | 39.8 | 46.9 | 13.3
| HCB | 30.7 | 46.7 | 22.6
| JPT | 43.4 | 43.4 | 13.3
| YRI | 98.6 | 1.4 | 0.0
| ASW | 66.7 | 33.3 | 0.0
| CHB | 30.7 | 46.7 | 22.6
| CHD | 34.9 | 45.0 | 20.2
| GIH | 38.6 | 44.6 | 16.8
| LWK | 87.3 | 11.8 | 0.9
| MEX | 22.4 | 55.2 | 22.4
| MKK | 82.1 | 16.7 | 1.3
| TSI | 24.5 | 57.8 | 17.6
| 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=A
  |Pval=8E-7
  |OR=1.31
  |ORtxt=[1.18-1.46]
  }}

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