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 inflammation of small blood vessels, often causing a skin rash.
causes an overactive spleen that removes too many blood cells.
is a rare genetic syndrome with wide-set eyes, hypospadias, and extra digits.
is a rare genetic condition affecting facial development before birth.
is a rare disorder causing wide-set eyes, ear pits, and hearing loss.
is high blood pressure, often silent, raising heart, stroke, kidney risks.
causes inherited high blood pressure from overactive mineralocorticoid receptor signaling.
is a serious complication of very high blood pressure affecting brain function.
is heart damage caused by long-term high blood pressure.
is eye damage caused by high blood pressure affecting retinal blood vessels.
is an overactive thyroid causing high hormone levels and rapid metabolism.
is a condition with unusually high thyroid hormone levels in the blood.
is a rare, usually harmless condition causing excess hair on the elbows.
is a rare genetic condition causing excessive soft hair growth.
causes unusually excessive hair growth on the eyelids.
is a rare genetic disorder causing excessive hair growth and bone changes.
is a genetic heart muscle thickening causing chest pain and arrhythmias.
is a genetic subtype with heart muscle thickening and arrhythmias.
causes thickened heart muscle, affecting pumping and rhythm; often inherited.
is a genetic heart condition where heart muscle thickens and stiffens.
is an inherited heart condition that thickens the heart muscle.
is a genetic heart muscle disease causing thickened walls and rhythm problems.
is an inherited heart muscle disease that can affect breathing and rhythm.
is an inherited heart condition causing thickened heart muscle and rhythm problems.