{{Rsnum
|rsid=499590
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=LOC101054525
|position=101143195
|Gene_s=LOC101054525
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 44.2 | 50.4 | 5.3
| HCB | 98.5 | 1.5 | 0.0
| JPT | 97.3 | 2.7 | 0.0
| YRI | 40.8 | 46.3 | 12.9
| ASW | 32.1 | 53.6 | 14.3
| CHB | 98.5 | 1.5 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 55.4 | 33.7 | 10.9
| LWK | 38.2 | 45.5 | 16.4
| MEX | 72.4 | 25.9 | 1.7
| MKK | 42.6 | 47.1 | 10.3
| TSI | 31.7 | 49.5 | 18.8
| HapMapRevision=28
}}Part of a haplotype, standalone effect is ambiguous.
{{PMID Auto GWAS
|PMID=20547493
|Trait=Ovarian cancer
|Title=Genetic variation in the progesterone receptor gene and risk of endometrial cancer: a haplotype-based approach.
|RiskAllele=C
|Pval=0.010
|OR=0.95
|ORtxt=[0.81-1.12]
|OA=1
}}

{{on chip | Illumina Human 1M}}