{{Rsnum
|rsid=17112190
|Gene=LCOR
|Chromosome=10
|position=98639846
|Orientation=plus
|GMAF=0.118
|Gene_s=LCOR
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 11.5 | 88.5
| HCB | 0.0 | 0.7 | 99.3
| JPT | 0.0 | 8.0 | 92.0
| YRI | 9.5 | 42.9 | 47.6
| ASW | 7.0 | 52.6 | 40.4
| CHB | 0.0 | 0.7 | 99.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 5.9 | 94.1
| LWK | 13.6 | 49.1 | 37.3
| MEX | 1.7 | 12.1 | 86.2
| MKK | 15.4 | 45.5 | 39.1
| TSI | 0.0 | 14.7 | 85.3
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23502783
  |Trait=Multiple myeloma (IgH translocation)
  |Title=The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
  |RiskAllele=A
  |Pval=9E-7
  |OR=1.80
  |ORtxt=[1.42-2.27]
  }}

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