{{Rsnum
|rsid=16879765
|Gene=EPDR1
|Chromosome=7
|position=37949493
|Orientation=plus
|GMAF=0.124
|Gene_s=EPDR1
|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 | 90.9 | 9.1 | 0.0
| HCB | 80.3 | 19.0 | 0.7
| JPT | 83.0 | 17.0 | 0.0
| YRI | 67.3 | 26.5 | 6.1
| ASW | 66.7 | 31.6 | 1.8
| CHB | 80.3 | 19.0 | 0.7
| CHD | 86.1 | 13.0 | 0.9
| GIH | 66.3 | 30.6 | 3.1
| LWK | 72.7 | 27.3 | 0.0
| MEX | 79.3 | 20.7 | 0.0
| MKK | 86.8 | 13.2 | 0.0
| TSI | 84.3 | 15.7 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21732829
|Trait=None
|Title=Wnt signaling and Dupuytren's disease.
|RiskAllele=A
|Pval=6E-39
|OR=1.9800
|ORtxt=None
}}

{{PMID Auto
|PMID=24089297
|Title=Common variants of the EPDR1 gene and the risk of Dupuytren’s disease
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}