rs1042838
A SNP in the PGR gene on chromosome 11. Its most notable genotype is A;A: 1.42x risk for endometrial ovarian cancer; overlaps with rs608995
- Gene
- PGR
- Location
- Chr 11101,062,681 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 10%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- C;CGoodnormal risk
- A;CBad1.28x risk for endometrial ovarian cancer; overlaps with rs608995
- A;AMost notableBad1.42x risk for endometrial ovarian cancer; overlaps with rs608995
SNPedia records rs1042838 on the minus strand: (G;G), (G;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageC;C 89% A;C 10% A;A 1%
- European ancestry (Utah)C;C 66% A;C 29% A;A 5%
- Han Chinese (Beijing)C;C 98% A;C 2% A;A 0%
- Japanese (Tokyo)C;C 100% A;C 0% A;A 0%
- Yoruba (Nigeria)C;C 100% A;C 0% A;A 0%
- African ancestry (Southwest US)C;C 97% A;C 4% A;A 0%
- Chinese (Denver)C;C 98% A;C 2% A;A 0%
- Gujarati IndianC;C 87% A;C 13% A;A 0%
- Luhya (Kenya)C;C 99% A;C <1% A;A 0%
- Mexican ancestry (Los Angeles)C;C 71% A;C 26% A;A 3%
- Maasai (Kenya)C;C 92% A;C 8% A;A 0%
- TuscanC;C 67% A;C 29% A;A 4%
Related
Conditions, medicines and genes
Other PGR SNPs
Genosets
- Gs287Progesterone receptor gene PROGINS haplotypeImportant
- Gs286Possibility of progesterone receptor gene haplotype with 1.98x endometrial cancer risk.Worth knowing
Genosets combine several genotypes. Twofold checks them in your report.
Notes
From SNPedia
Show notes, about 370 words
Minor allele (T) of this SNP uniquely identifies what is known as the PROGINS allele in the progresterone receptor gene PGR. Two SNP's tagging a partial haplotype of the PGR gene were associated with an increased risk of ovarian cancer among homozygous carriers as compared with noncarriers: rs1042838 (PROGINS allele; odds ratio [OR] = 3.23, 95% confidence interval [CI] = 1.19 to 8.75, P = .022) and rs608995 (minor allele; OR = 3.10, 95% CI = 1.63 to 5.89, P 90% power to detect OR 1.3 for this SNP, so if an effect exists it must be quite small. A pooled analysis of 4788 ovarian cancer cases and 7614 controls in 2008 suggested that PROGINS risk is limited to invasive endometrioid subtype , to that effect a 2010 study found association with endometrial cancer with same risk haplotypes as the earlier haplotype study on ovarian cancer. A 2014 metastudy however did find association between PROGINS and ovarian cancer, but statistically significant only for Caucasians, those having never used oral contraceptives, and serous (endometrial) cancers, while another meta-study looking at endometrial cancer specifically found association (OR 1.52-2.72, p = 0.0008-0.03) among European women in particular. This SNP has also been reported to be associated with migraine-associated vertigo (p = 0.0007). SNPs in genes involved in female hormonal pathways have been a subject of particular interest in the study of migraines because females appear to be more prone to migraines than males. Previous studies had suggested that the minor allele of this SNP might also influence breast cancer. However, a 2009 European study of 30,000 breast cancer cases, compared to 30,000 controls, found no association, or as they put it, "persuasive evidence against an overall association between invasive breast cancer risk and (this SNP)". Association of the progesterone receptor gene polymorphism (PROGINS) with endometriosis: a meta-analysis. Progesterone receptor PROGINS and +331G/A polymorphisms confer susceptibility to ovarian cancer: a meta-analysis based on 17 studies. Association of progesterone receptor with migraine-associated vertigo Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium.
Source and license
Adapted from rs1042838 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.