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 rare cancer in the chest area's soft tissues.
is a rare tumor in the chest containing different tissue types.
is a rare inherited bleeding disorder with unusually large platelets.
is an inherited disorder that makes it hard to break down fats.
is a rare inherited disorder causing developmental, neurologic, skin, and gastrointestinal problems.
affects the inner part of an organ, often the kidneys.
is a rare colon cancer subtype that often has distinctive cells.
is a usually harmless kidney condition with tiny cysts in collecting ducts.
is a rare thyroid cancer arising from calcitonin-producing C cells.
is an overactive adrenal gland condition causing excess adrenaline and related symptoms.
is a fast-growing brain tumor that usually starts in the cerebellum.
is a fast-growing childhood brain tumor subtype that often spreads.
is a fast-growing childhood brain tumor subtype affecting the cerebellum.
is a fast-growing brain tumor driven by abnormal Sonic Hedgehog signaling.
is a fast-growing brain tumor subtype linked to TP53 gene changes.
is a type of childhood brain cancer driven by SHH pathway changes.
is a rare childhood brain tumor, often with better treatment outcomes.
is a rare brain tumor subtype that usually responds well to treatment.
is a rare central nervous system tumor that mainly affects children.
is a rare inherited eye condition affecting the cornea's outer layer.
is a rare inherited eye condition affecting the cornea’s outer layer.
is an inherited eye condition affecting the cornea's outer layer.
is a genetic connective tissue disorder that can affect the aorta.
is a usually harmless enlargement of a fluid-filled space in the brain.