rs1937506
A SNP on chromosome 13. Its most notable genotype is A;A: 1.6x risk
- Gene
- None listed
- Location
- Chr 1367,461,239 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 22%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A), (A;G), (G;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 5% A;G 33% G;G 62%
- European ancestry (Utah)A;A 5% A;G 42% G;G 53%
- Han Chinese (Beijing)A;A 2% A;G 27% G;G 72%
- Japanese (Tokyo)A;A 5% A;G 31% G;G 64%
- Yoruba (Nigeria)A;A 3% A;G 22% G;G 75%
- African ancestry (Southwest US)A;A 7% A;G 35% G;G 58%
- Chinese (Denver)A;A <1% A;G 24% G;G 75%
- Gujarati IndianA;A 9% A;G 36% G;G 55%
- Luhya (Kenya)A;A 2% A;G 30% G;G 68%
- Mexican ancestry (Los Angeles)A;A 14% A;G 43% G;G 43%
- Maasai (Kenya)A;A 8% A;G 37% G;G 56%
- TuscanA;A 3% A;G 39% G;G 58%
Related
Conditions, medicines and genes
Notes
From SNPedia
Show notes, about 210 words
rs1937506 has been reported in a large study to be associated with high blood pressure. The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.33 (CI 1.04-1.69), and for homozygotes, 1.60 (CI 1.26-2.02). As follows from results of Replication of the Wellcome Trust genome-wide association study of essential hypertension this SNP (rs1937506) only one of the top 6 SNPs which might be associated with essential hypertension in Americans of European origin. This SNP shows a significant but opposite effect in Americans of Hispanic origin. Each additional G allele of rs1937506 is associated with a 24.9 mmHg decrease of systolic blood pressure (SBP) in European Americans and with a 27.7 mmHg increase in Hispanic Americans. Considering diastolic blood pressure (DBP) each additional G allele is associated with a 8.7 mmHg decrease of DBP in European Americans, whereas the results are non-significant for Hispanic Americans. http://www.ncbi.nlm.nih.gov/pubmed/18523456?ordinalpos=&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.SmartSearch&log$=citationsensor PMID 18523456 Dissecting complex traits: recent advances in hypertension genomics. Novel genetic variations associated with salt sensitivity in the Korean population.
Source and license
Adapted from rs1937506 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.