rs2032582 is a genetic variant on gene ABCB1 associated with Inflammatory bowel disease 13.
rs10876864 is a genetic variant on gene IKZF4 associated with Intelligence and Allergic disease.
rs11540652 is a genetic variant on gene TP53 associated with Li-fraumeni syndrome 1 and Multiple myeloma.
rs104894226 is a genetic variant on gene HRAS associated with Costello syndrome and Large congenital melanocytic nevus.
rs7274581 is a genetic variant associated with Alzheimer's disease.
rs10808546 is a genetic variant associated with Abdominal aortic aneurysm.
is an inherited disorder causing phenylalanine buildup that can harm the brain.
is a rare inherited disorder affecting how the body makes certain fats.
is a rare inherited disorder affecting brain development and fat production.
is a rare inherited disorder that mainly affects the peripheral nerves.
is a rare inherited disorder affecting muscle and fat molecule production.
is a rare inherited disorder affecting plasmalogen production and many body systems.
is a group of disorders affecting heme production and causing symptoms.
is a rare inherited condition affecting how the body breaks down proline.
is a rare inherited disorder affecting how the body processes proteins.
is a rare inherited disorder affecting how the body modifies proteins.
is a rare inherited disorder affecting brain chemicals and phenylalanine processing.
is a rare inherited disorder affecting how the body breaks down purines.
is a group of inherited disorders affecting how the body handles nucleotides.
is a rare inherited condition affecting how the body uses vitamin B6.
is a rare inherited disorder affecting how the body processes pyrimidines.
is a rare inherited disorder affecting serine or glycine production and use.
is a rare inherited condition affecting how the body processes sialic acid.
is a rare inherited disorder affecting glutathione production and the body's defenses.
is a rare inherited condition affecting how the body uses thiamine.
is a rare inherited condition affecting how the body processes tryptophan.
is a rare inherited condition affecting how the body breaks down tyrosine.
is a rare inherited disorder causing dangerous ammonia buildup in the blood.
is a rare inherited disorder affecting how vitamins and cofactors are absorbed.
is a rare condition affecting how the body absorbs and uses zinc.