rs471767
A SNP in the PGR gene on chromosome 11. Its most notable genotype is A;G.
- Gene
- PGR
- Location
- Chr 11101,034,566 (GRCh38)
- Highest magnitude
- 0.1Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 23%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A), (A;G). 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.
- AverageA;A 61% A;G 33%
- European ancestry (Utah)A;A 47% A;G 45%
- Han Chinese (Beijing)A;A 90% A;G 10%
- Japanese (Tokyo)A;A 89% A;G 10%
- Yoruba (Nigeria)A;A 50% A;G 42%
- African ancestry (Southwest US)A;A 37% A;G 51%
- Chinese (Denver)A;A 92% A;G 7%
- Gujarati IndianA;A 44% A;G 45%
- Luhya (Kenya)A;A 60% A;G 34%
- Mexican ancestry (Los Angeles)A;A 71% A;G 28%
- Maasai (Kenya)A;A 49% A;G 44%
- TuscanA;A 39% A;G 48%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
news The effectiveness of 17 alpha-hydroxyprogesterone caproate for prevention of recurrent preterm birth is influenced by SNPs. Black women *rs471767 homozygous for the major allele treatment significantly reduced the rate of preterm birth. *rs578029 who had a least one copy of the major allele, treatment significantly reduced in preterm birth non-black women *a least one copy of the minor allele of rs503362 had a significant reduction with treatment *with at least one copy of the minor allele of rs666553 had a significant reduction in very preterm birth
Source and license
Adapted from rs471767 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.