rs149899650
Variant in the KCNJ2 gene (Potassium Inwardly Rectifying Channel Subfamily J Member 2 (Kir2.1))
rs149899650 is a single nucleotide polymorphism (SNP) in the KCNJ2 gene, involved in cardiac inward rectifier / resting potential. 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 rs149899650 variant?
rs149899650 is a SNP (single nucleotide polymorphism) in the KCNJ2 (Potassium Inwardly Rectifying Channel Subfamily J Member 2 (Kir2.1)) gene. It belongs to the Cardiovascular category and is part of the Autonomic Nervous System biological cluster. KCNJ2 encodes Kir2.1, an inward rectifier K+ channel maintaining the cardiac resting membrane potential; mutations cause Andersen-Tawil syndrome.
Biological role and pathway
This variant sits within the KCNJ2 gene, which is involved in the cardiac inward rectifier / resting potential 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.
rs149899650 and Long COVID / ME-CFS research
Kir2.1 dysfunction causes periodic paralysis and arrhythmias; variants may affect cardiac resting potential and contribute to arrhythmias in Long COVID.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: KCNJ2
rs149899650 is one of 1 known variant in the KCNJ2 gene. To understand the full biological context of this variant, explore the parent gene page.
View KCNJ2 gene page →Conditions studied in relation to rs149899650
Research into KCNJ2 variants including rs149899650 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 KCNJ2 and the rs149899650 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.
Frequently asked questions
What is the rs149899650 variant in the KCNJ2 gene?
rs149899650 is a single nucleotide polymorphism (SNP) located in the KCNJ2 (Potassium Inwardly Rectifying Channel Subfamily J Member 2 (Kir2.1)) gene, which is involved in cardiac inward rectifier / resting potential. KCNJ2 encodes Kir2.1, an inward rectifier K+ channel maintaining the cardiac resting membrane potential; mutations cause Andersen-Tawil syndrome.
How may the rs149899650 variant relate to Long COVID or ME/CFS?
Kir2.1 dysfunction causes periodic paralysis and arrhythmias; variants may affect cardiac resting potential and contribute to arrhythmias in Long COVID.
Can a consumer DNA test detect the rs149899650 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.
Find out if you carry the rs149899650 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.
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References
The following publications were used in compiling the research context for KCNJ2 and its variants. This is not an exhaustive literature review.
- [1]PMID: 32966261
- [2]Nature Genetics
- [3]NEJM