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rs3740753

From SNPedia

Orientationplus
Stabilizedplus
Make rs3740753(C;C)
Make rs3740753(C;G)
Make rs3740753(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position101128040
GeneLOC101054525, PGR
is asnp
is mentioned by
dbSNPrs3740753
ebirs3740753
HLIrs3740753
Exacrs3740753
Varsomers3740753
Maprs3740753
PheGenIrs3740753
hapmaprs3740753
1000 genomesrs3740753
hgdprs3740753
ensemblrs3740753
gopubmedrs3740753
geneviewrs3740753
scholarrs3740753
googlers3740753
pharmgkbrs3740753
gwascentralrs3740753
openSNPrs3740753
23andMers3740753
23andMe allrs3740753
SNP Nexus

SNPshotrs3740753
SNPdbers3740753
MSV3drs3740753
GWAS Ctlgrs3740753
Max Magnitude
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 21600550OA-icon.png]

PROGINS allele and this SNP in particular were found to not be involved in male infertility. [PMID 23934021OA-icon.png]

GWAS snp
PMID [PMID 20547493OA-icon.png]
Trait Endometrial cancer
Title Genetic variation in the progesterone receptor gene and risk of endometrial cancer: a haplotype-based approach.
Risk Allele G
P-val 0.40
Odds Ratio 1.25 [1.03-1.54]

[PMID 23934021OA-icon.png] Association of progesterone receptor gene polymorphism with male infertility and clinical outcome of ICSI

[PMID 21600550OA-icon.png] 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