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 a common, treatable anemia from low iron causing fatigue and breathlessness.
affects how your body absorbs, uses, stores, or loses iron.
causes blurred or distorted vision from an unevenly curved cornea.
is a disorder of the large intestine causing pain and bowel changes.
causes skin inflammation from contact with irritating substances like soaps or chemicals.
is a rare eye disease causing retinal inflammation and possible vision loss.
is a rare nerve disorder causing muscle stiffness, twitching, and cramps.
is reduced blood flow that can damage tissues and organs.
is bone damage caused by reduced blood flow to the bone.
is reduced blood flow to the colon, causing pain and bloody stools.
is a rare benign soft-tissue growth caused by prolonged pressure.
is nerve damage caused by reduced blood flow to the nerves.
is a rare genetic condition affecting the spine, pelvis, and growth.
is a rare tumor in the pancreas that can affect hormone levels.
is a rare inherited disorder affecting how the body breaks down valine.
is a rare Y chromosome change that can affect sex development.
is a rare Y chromosome change with extra short-arm material.
is a rare Y chromosome change affecting male development and fertility.
is an asthma type triggered by allergy to isocyanate chemicals.
is an inherited immune disorder causing very low antibodies and recurrent infections.
is a rare birth condition where the gallbladder never develops.
is a rare birth difference where a limb is missing.
is a severe birth defect where the brain does not fully form.
is a severe birth defect causing incomplete brain and skull development.