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 blood cancer of the lymphatic system in children, often curable.
is a rare childhood soft-tissue cancer of blood vessel support cells (pericytes).
is a rare childhood soft tissue cancer affecting multiple tissue types.
is a rare, aggressive nerve sheath cancer (MPNST) in children.
is a usually benign ovarian growth (germ cell tumor) in children.
is a nerve-related mediastinal tumor in children, benign or cancerous.
is a fast-growing brain tumor in the cerebellum, often spreading.
is a rare, often benign brain or spinal meningeal tumor in children.
is a rare, fast-growing pediatric cancer of bone and soft tissues.
is a rare noncancerous (benign) kidney tumor with many cysts, usually curable.
is a rare pediatric soft-tissue cancer with cartilage-like, myxoid tumors.
is a rare childhood brain tumor affecting the optic nerve, impairing vision.
is a brain tumor affecting the optic pathway, impairing vision in children.
is a fast-growing bone cancer in children and teens; often treatable.
is a rare ovarian germ cell cancer, usually curable with treatment.
is a rare, aggressive ovarian germ cell cancer in children.
is a rare ovarian germ cell cancer in children, often treatable.
is a rare pediatric ovarian cancer from germ cells, often treatable.
is a rare, slow-growing bone surface cancer in children’s long bones.
is a slow-growing, usually benign brain tumor (low-grade glioma) in children.
is a rare, aggressive skeletal muscle cancer affecting children.
is an abnormal spinal cord growth in children affecting nerves and movement.
is a rare, aggressive pediatric supratentorial brain cancer with C19MC alterations.
is a childhood brain tumor above the tentorium causing headaches, seizures, weakness.