{{Rsnum
|rsid=3740753
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=PGR
|position=101128040
|Gene_s=LOC101054525,PGR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}Part of a haplotype [[Gs286]], standalone effect for [[endometrial cancer]] is ambiguous. Tightly linked with [[PROGINS]] [[allele]].

Some evidence of interaction on caucasian/hispanic patients with 17-alpha-hydroxyprogesterone caproate for reducing recurrent preterm birth detected. {{PMID|21600550|OA=1
}}

[[PROGINS]] [[allele]] and this [[SNP]] in particular were found to not be involved in [[male infertility]]. {{PMID|23934021}}

{{PMID Auto GWAS
|PMID=20547493
|Trait=Endometrial cancer
|Title=Genetic variation in the progesterone receptor gene and risk of endometrial cancer: a haplotype-based approach.
|RiskAllele=G
|Pval=0.40
|OR=1.25
|ORtxt=[1.03-1.54]
|OA=1
}}

{{PMID|23934021}} Association of progesterone receptor gene polymorphism with male infertility and clinical outcome of ICSI

{{PMID|21600550|OA=1
}} Progesterone receptor polymorphisms and clinical response to 17-alpha-hydroxyprogesterone caproate

{{PMID|15632380}} Clarifying the PROGINS allele association in ovarian and breast cancer risk: a haplotype-based analysis