rs1050700

Variant in the SDHA gene (Succinate Dehydrogenase Complex Flavoprotein Subunit A)

rs1050700 is a single nucleotide polymorphism (SNP) in the SDHA gene, involved in TCA cycle / electron transport chain complex II. 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 rs1050700 variant?

rs1050700 is a SNP (single nucleotide polymorphism) in the SDHA (Succinate Dehydrogenase Complex Flavoprotein Subunit A) gene. It belongs to the Metabolic category and is part of the Mitochondrial Energy Production & PEM biological cluster. SDHA encodes the catalytic subunit of complex II (succinate dehydrogenase), which links the TCA cycle to the electron transport chain.

Biological role and pathway

This variant sits within the SDHA gene, which is involved in the TCA cycle / electron transport chain complex II pathway. Genes within the Mitochondrial Energy Production & PEM 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.

rs1050700 and Long COVID / ME-CFS research

Complex II dysfunction affects oxidative phosphorylation efficiency; SDHA variants may contribute to mitochondrial energy deficits and post-exertional symptoms in Long COVID.

This information is based on published research and does not constitute medical advice. See references below.

Parent gene: SDHA

rs1050700 is one of 1 known variant in the SDHA gene. To understand the full biological context of this variant, explore the parent gene page.

View SDHA gene page →

Conditions studied in relation to rs1050700

Research into SDHA variants including rs1050700 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 SDHA and the rs1050700 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 SDHA gene

The following variants in SDHA are also studied in relation to chronic illness and may be analysed together for a more complete picture.

Frequently asked questions

What is the rs1050700 variant in the SDHA gene?

rs1050700 is a single nucleotide polymorphism (SNP) located in the SDHA (Succinate Dehydrogenase Complex Flavoprotein Subunit A) gene, which is involved in TCA cycle / electron transport chain complex II. SDHA encodes the catalytic subunit of complex II (succinate dehydrogenase), which links the TCA cycle to the electron transport chain.

How may the rs1050700 variant relate to Long COVID or ME/CFS?

Complex II dysfunction affects oxidative phosphorylation efficiency; SDHA variants may contribute to mitochondrial energy deficits and post-exertional symptoms in Long COVID.

Can a consumer DNA test detect the rs1050700 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 rs1050700 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 Report

Informational and educational only · Not a diagnostic tool · GDPR compliant

References

The following publications were used in compiling the research context for SDHA and its variants. This is not an exhaustive literature review.

  • [1]PMID: 34316049
  • [2]Nature Genetics
  • [3]Cell Metabolism