snp

Full title: A comparison of genome-wide association analyses of persistent symptoms after Lyme disease, fibromyalgia, and myalgic encephalomyelitis – chronic fatigue syndrome Annemarie G. Hirsch, Anne E. Justice, Amy Poissant, Cara M. Nordberg, Navya S. Josyula, John Aucott, Alison W. Rebman &...

Preprint posted on MedRxiv, now posted with new title on SSRN, see post #4 Integrative Genome-Wide Association Studies of COVID-19 Susceptibility and Hospitalization Reveal Risk Loci for Long COVID Zhongshan Cheng Abstract Long COVID presents a significant public health challenge...

Actively Protective Combinatorial Analysis: a Scalable Novel Method for Detecting Variants that Contribute to Reduced Disease Prevalence in High-Risk Individuals Jason Sardell; Sayoni Das; Krystyna Taylor; Colin Stubberfield; Andy Malinowski; Mark Strivens; Steve Gardner We present a novel...

Genetic variants associated with chronic fatigue syndrome predict population-level fatigue severity and actigraphic measurements Liu, Patrick Z; Raizen, David M; Skarke, Carsten; Brooks, Thomas G; Anafi, Ron C STUDY OBJECTIVES The diagnosis of myalgic encephalomyelitis/chronic fatigue syndrome...

Bioinformatic analysis predicts the regulatory function of noncoding SNPs associated with Long COVID-19 syndrome Maiti, Amit K. Long or Post COVID-19 is a condition of collected symptoms persisted after recovery from COVID-19. Host genetic factors play a crucial role in developing Long...

A saturated map of common genetic variants associated with human height Loic Yengo and others (multiple) Abstract Common single-nucleotide polymorphisms (SNPs) are predicted to collectively explain 40–50% of phenotypic variation in human height, but identifying the specific variants and...

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3442958/

Full title: No replication of previously reported association with genetic variants in the T cell receptor alpha (TRA) locus for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) Abstract Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a disease with a variety of...

Genetic testing can be performed with a device called SNP chip. Not all genetic testing is done with these. Direct-to-consumer genetic testing companies like 23andME often use SNP chips. A problem with SNP chips is that they are unreliable when it comes to rare gene variants. There is the risk...

Apparently most of the population have variants or absence of the CYP2C19 gene. But how do I figure out from the raw genetic data (rs17878459 etc numbers, and alleles) which variants I do or don't have? I'm working from SNPedia but usually it's just a case of checking the rs number, and...

https://www.medrxiv.org/content/10.1101/2020.10.27.20220939v1 Threads on genetic risks listed here: https://www.s4me.info/threads/evidence-for-a-genetic-component-in-me-cfs-discussion-thread.16117/#post-277072

Dear All, I am preparing an email to a number of researchers for the gene called ABCC6. Looking for further information regarding its function, one can find that it is a gene responsible for Pseudoxanthoma Elasticum (PXE) but the techniques i use suggest otherwise, meaning it should be further...

Background The metabolic trap hypothesis being investigated by the OMF is currently investigating IDO2, with the Severely Ill Big Data Project finding IDO2 mutations in the 20 patients ill with M.E. This question is about how someone can check if they have the mutations found based on genetic...

Wall Street Journal: The Unfulfilled Promise of DNA Testing The article weaves the story of a young sick girl thru it by discussing how genetic testing has resulted in her diagnosis changing over and over and over as the science changes constantly. And how this is happening to other patients...

This is a preprint - made available by the authors on bioRxiv before publication while the paper is still in peer review.