rs1048101
Variant in the ADRA1A gene (Adrenoceptor Alpha 1A)
rs1048101 is a single nucleotide polymorphism (SNP) in the ADRA1A gene, involved in adrenergic receptor signaling. Variants at this position have been studied in relation to immune function, metabolism, and chronic illness.
This page is for educational and informational purposes only. Not a diagnostic tool. Always consult a qualified healthcare provider.
What is the rs1048101 variant?
rs1048101 is a SNP (single nucleotide polymorphism) in the ADRA1A (Adrenoceptor Alpha 1A) gene. It belongs to the Autonomic category and is part of the Autonomic Nervous System biological cluster. ADRA1A encodes the alpha-1A adrenergic receptor, which mediates vasoconstriction and smooth muscle contraction.
Biological role and pathway
This variant sits within the ADRA1A gene, which is involved in the adrenergic receptor signaling pathway. Genes within the Autonomic Nervous System cluster work together to maintain balanced function across interconnected biological systems.
Variants in genes within this pathway may influence an individual's predisposition to altered function — particularly under conditions of physiological stress such as viral infection or prolonged illness.
rs1048101 and Long COVID / ME-CFS research
ADRA1A variants may influence vascular tone regulation and contribute to blood pressure instability seen in Long COVID dysautonomia.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: ADRA1A
rs1048101 is one of 1 known variant in the ADRA1A gene. To understand the full biological context of this variant, explore the parent gene page.
View ADRA1A gene page →Conditions studied in relation to rs1048101
Research into ADRA1A variants including rs1048101 has explored associations with the following conditions. These are areas of scientific investigation and do not imply causation.
Genetic insights from DNA data
Consumer DNA files from 23andMe, AncestryDNA, and MyHeritage contain raw SNP data. When you upload your file to ChronicDNA, the analysis engine checks your genotype against a curated panel of 80+ genes selected for their relevance to Long COVID, ME/CFS, and connected biological pathways - some of which may include ADRA1A and the rs1048101 variant.
The report is educational - it explains which variants you carry, what the research says about them, and how they fit into the biological pathways most relevant to chronic illness. Results are presented in plain English with appropriate scientific context, no medical jargon, no scare tactics. All results should be discussed with a qualified healthcare provider.
Other variants in the ADRA1A gene
The following variants in ADRA1A are also studied in relation to chronic illness and may be analysed together for a more complete picture.
Frequently asked questions
What is the rs1048101 variant in the ADRA1A gene?
rs1048101 is a single nucleotide polymorphism (SNP) located in the ADRA1A (Adrenoceptor Alpha 1A) gene, which is involved in adrenergic receptor signaling. ADRA1A encodes the alpha-1A adrenergic receptor, which mediates vasoconstriction and smooth muscle contraction.
How may the rs1048101 variant relate to Long COVID or ME/CFS?
ADRA1A variants may influence vascular tone regulation and contribute to blood pressure instability seen in Long COVID dysautonomia.
Can a consumer DNA test detect the rs1048101 variant?
Many consumer DNA tests such as 23andMe, AncestryDNA, and MyHeritage genotype common SNPs. ChronicDNA analyses your raw DNA file and reports on variants studied in relation to chronic illness, immune function, and metabolism. This is not a diagnostic service — results are informational and educational only.
Related articles
- Long COVID Dysautonomia: What Your Genes May Reveal
Explore how genes in the autonomic nervous system may relate to Long COVID dysautonomia, including POTS, heart rate changes and orthostatic intolerance.
- Long COVID POTS: Symptoms, Testing and Genetics
Learn how Long COVID POTS affects heart rate, how standing and tilt table tests assess it, and which genes research is exploring.
Find out if you carry the rs1048101 variant
Upload your DNA data from 23andMe, AncestryDNA, or MyHeritage and receive a personalised report covering >80 genes relevant to Long COVID and ME/CFS.
Get Your Personalised DNA ReportInformational and educational only · Not a diagnostic tool · GDPR compliant
References
The following publications were used in compiling the research context for ADRA1A and its variants. This is not an exhaustive literature review.
- [1]PMID: 33948838
- [2]Nature Genetics
- [3]Journal of Clinical Investigation