rs1042714
A SNP in the ADRB2 gene on chromosome 5. Its most notable genotype is C;C: normal
- Gene
- ADRB2
- Location
- Chr 5148,826,910 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 24%
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CMost notableGoodnormal
- C;GNot ratedcomplex; see details for increased risks
- G;GNot ratedcomplex; see details for increased risks
On SNPedia: (C;C), (C;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 4 HapMap populations.
- AverageC;C 68% C;G 23% G;G 9%
- European ancestry (Utah)C;C 39% C;G 31% G;G 31%
- Han Chinese (Beijing)C;C 76% C;G 24% G;G 0%
- Japanese (Tokyo)C;C 86% C;G 11% G;G 2%
- Yoruba (Nigeria)C;C 71% C;G 24% G;G 5%
Related
Conditions, medicines and genes
Other ADRB2 SNPs
Genosets
- Gs284any diet works for youWorth knowing
- Gs285claimed to lose 2.5x as much weight on a low fat dietWorth knowing
Genosets combine several genotypes. Twofold checks them in your report.
Notes
From SNPedia
Show notes, about 270 words
Several susceptibilities have been linked to rs1042714, a SNP in the ADRB2 gene that is also known as the Q27E SNP. The rs1042714(C) allele encodes the glutamine (Gln; "Q"), and the rs1042714(G) allele encodes the glutamic acid (Glu; "E"). A study of 304 patients found that the Glu27 allele led to increased risk for idiopathic venous thromboembolism; the reported odds ratio was 1.40 (CI: 1.09-1.79, p=0.006) for carriers of at least one risk allele. A study of 334 families with at least one child with autism found that increased risk associated with the rs1042714(G;G) homozygous genotype; the odds ratio reported was between 1.33-1.60 (CI: 1.07-2.58). The risk was approximately doubled among mothers who had clinical markers for pregnancy related stress. In a study of 342 patients with type-2 diabetes, the rs1042714(G;G) genotype was associated with reduced risk compared to carriers of a rs1042714(C) allele, with an odds ratio of 0.56 (CI: 0.36-0.91). A study of 294 Italian ischemic stroke patients found increased risk associated with the rs1042714(G;G) genotype, with an odds ratio of 1.68 (CI: 1.17-2.41, p=0.005). A large study of almost 8,000 patients found no consistent evidence for association with obesity, type-2 diabetes or hypertension, however, there was some association between the rs1042714(G) allele and systolic blood pressure. Among 215 adults treated with topical beta-blockers to reduce intraocular pressure (IOP), rs1042714(C;C) genotypes were significantly more likely to experience a (desirable) IOP decrease of 20% or more (odds ratio 2.00, CI: 1.00-4.02).
Source and license
Adapted from rs1042714 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.