rs1801253

A SNP in the ADRB1 gene on chromosome 10. Its most notable genotype is C;C: responds well to bucindolol; may also depend on rs1801252

Gene
ADRB1
Location
Chr 10114,045,297 (GRCh38)
Highest magnitude
1.1Minor
Tested on
23andMe, AncestryDNA
Minor allele frequency
30%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableNot ratedresponds well to bucindolol; may also depend on rs1801252Minor · 1.153% of people
  2. C;GNot rateddepends on rs1801252Typical · 0.038% of people
  3. G;GGooddepends on rs1801252Typical · 0.09% of people

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 53% C;G 38% G;G 9%
  • European ancestry (Utah)C;C 51% C;G 37% G;G 12%
  • Han Chinese (Beijing)C;C 55% C;G 41% G;G 5%
  • Japanese (Tokyo)C;C 74% C;G 21% G;G 5%
  • Yoruba (Nigeria)C;C 32% C;G 52% G;G 16%

Genosets

Genosets combine several genotypes. Twofold checks them in your report.

Notes

From SNPedia

Show notes, about 380 words

Also known as Arg389, variation at this SNP, located in the ADRB1 gene, may encode either the amino acid glycine or arginine at amino acid position 389 of the corresponding protein, the beta-1 adrenergic receptor (hence why it is frequently called Arg389Gly). This protein is the target of beta blocker drugs, and so how well the drug works to help lower a patients high blood pressure depends in part on this SNP. The status of this SNP is often reported together with the status of SNP rs1801252, which encodes an amino acid variant at position 49 of the same (ADRB1) protein. The rs1801253(G) allele encodes the glycine. One of the best known studies of the effects of these 2 separate SNPs on the average efficacy of the beta blocker metoprolol in lowering blood pressure (BP) can be summarized for patients with the corresponding genotypes as follows : *rs1801252(A;A) and rs1801253(C;C) carriers: 15 point drop in BP *rs1801252(A;G) and rs1801253(C;C) carriers: 9 point drop in BP *rs1801252(A;A) and rs1801253(C;G) carriers: 6 point drop in BP *rs1801252(A;G) and rs1801253(C;G) carriers: <1 point drop in BP This SNP may also determine whether the drug bucindolol will have any effect on a particular patient. In a separate study of 600+ women initially referred for coronary angiography and then followed for 6 years, during which time 115 experienced a heart problem, rs1801253(G;G) individuals were calculated to be at higher risk (adjusted hazard ratio 3.63, CI: 1.17&#226;&#8364;&#8220;11.28). This risk was specifically for myocardial infarction, and was only seen in women without obstructive coronary artery disease. Other press releases or articles include: * Alters response to heart failure drugs bisoprolol, metoprolol, and carvedilol eurekalert.org * This press release provides a helpful summary of the PMID 16844790| research paper]. * Patent filings, such as USPTO application 20060177838 and others, include claims that "being homozygous in the .beta..sub.1AR gene to encode an arginine at position 389 {ie rs1801253} in the gene product provides the patient with a physiology that is amenable to treatment with bucindolol." (This is a SNP in a different gene.) Beta-Blocker Response

Source and license

Adapted from rs1801253 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.