THE PURSER WELLNESS ENCYCLOPEDIA
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What’s searchable?…ce a form of folate used in the processing of homocysteine. Common variants are different from rare variants that cause severe MTHFR deficiency. Topics: methionine, protein restriction, homocysteine, one-carbon metabolism, methylation, glu…
…ce a form of folate used in the processing of homocysteine. Common variants are different from rare variants that cause severe MTHFR deficiency. Topics: Skyrizi, risankizumab, IL-23, homocysteine, psoriasis, Crohn’s disease, ulcerative col…
…ce a form of folate used in the processing of homocysteine. Common variants are different from rare variants that cause severe MTHFR deficiency. Topics: IL-8, CXCL8, occult infection, persistent inflammation, homocysteine, cytokines
…ce a form of folate used in the processing of homocysteine. Common variants are different from rare variants that cause severe MTHFR deficiency. Topics: ulcerative colitis, Crohn’s disease, IBD, MTHFR, glutathione, probiotics, micronutrien…
Dr. Purser covers common terminology and phrases on MTHFR and genetics. Learn how MTHFR may be affecting how you feel! Contact us at (801) 796-7667 or info@danpursermd.com for help. Check back often for the newest updates!
Makes an enzyme that helps break down catechol compounds, including some neurotransmitters. A common variant does not by itself explain mood, attention or stress tolerance.
G6PC2 encodes a glucose-6-phosphatase-related protein expressed in pancreatic islet cells. Common variation is associated with differences in fasting glucose regulation; it is not the insulin receptor.
HFE helps regulate iron absorption through signaling that influences hepcidin. The commonly discussed C282Y and H63D variants correspond to rs1800562 and rs1799945. Their implications depend on the combination present and clinical findings.
NAT2 encodes N-acetyltransferase 2, which helps process certain drugs and other compounds. Combinations of variants can influence acetylation status; one SNP usually does not tell the entire story.
F9 encodes coagulation factor IX. Disease-causing variants can result in hemophilia B, an inherited bleeding disorder, but a panel marker is not equivalent to a confirmed disease-causing finding.
IL1B encodes interleukin-1 beta, a cytokine involved in inflammatory responses and fever. Its production and activation are regulated processes, not simply an on/off consequence of having a common SNP.
Explore rs2857261, rs1057972, natural killer cells, CD8+ T cells, and questions about high-expression variants.
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