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.
causes unusually high biliverdin levels in the blood, sometimes turning skin green.
is a high calcium level in the blood that can cause symptoms.
is a form of sarcoidosis that causes high calcium levels in blood.
is excessive buildup of tooth-root cementum, usually found on dental x-rays.
is a rare inherited disorder causing high cholesterol and sometimes gallstones.
is a rare genetic disorder that makes harmful blood clots more likely.
causes episodes of unusually tight muscles and painful stiffness.
is a rare genetic neurological disorder causing exaggerated startle and stiffness.
is a rare inherited disorder causing exaggerated startle responses and muscle stiffness.
is a rare genetic disorder causing exaggerated startle responses and seizures.
is a rare disorder with too many eosinophils causing organ damage.
is a rare condition causing recurring purple skin spots from inflamed vessels.
is abnormally high blood sugar, often from diabetes; needs prompt evaluation.
is a rare genetic condition causing cataracts and underactive ovaries or testes.
is a condition with too much homocysteine in the blood.
is a rare immune disorder causing repeated infections and high IgE levels.
is a rare inherited autoinflammatory disorder causing recurrent fevers and inflammation.
causes excess insulin to drive blood sugar dangerously low.
is a condition causing dangerously low blood sugar from excess insulin.
is a rare genetic disorder causing excess insulin and low blood sugar.
causes inherited episodes of low blood sugar from excess insulin release.