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Transcellular oxalate and Cl absorption in mouse intestine is mediated by the DRA anion exchanger Slc26a3, and DRA deletion decreases urinary oxalate

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In good agreement with this role, genome-wide association studies correlated SNPs occurring at the level of SLC16A9 gene, with carnitine, propionylcarnitine and urate levels in serum (Kolz et al., 2009

Many of the genetic variants that increase the relative risk of fibromyalgia are either related to overactivation of pain receptors (neurotransmitters, receptors for neurotransmitters, release of neurotransmitters) and/or increased activation of inflammation.[ref] A preprint genome-wide association study in 2025 looked at genetic data from more than 2 million people, finding multiple genes that were associated with an increased risk of a diagnosis of fibromyalgia