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, usually benign soft-tissue tumor arising from nerve lining cells.
is a slow-growing lymphoma that starts in tissues lining organs.
is a rare, aggressive cancer that usually starts in the nose.
is an aggressive eye cancer that has spread beyond the eyeball.
is a rare cancer that starts in soft tissues outside bone.
is a rare soft tissue cancer that forms bone outside bones.
is a type of endometriosis that grows outside the pelvic area.
is tuberculosis (TB) infection outside the lungs, affecting various organs.
is a group of movement disorders affecting coordination, muscle control, and posture.
is a rare cancer of soft tissues related to Ewing sarcoma.
is a rare cancer of soft tissues that forms cartilage-like tumors.
is a rare soft tissue cancer that often grows slowly.
is a rare disorder affecting heart rhythm, growth, skin, and head size.
is epilepsy that starts outside the brain's temporal lobes.
is a rare, usually slow-growing brain tumor that forms outside the ventricles.
is a lung inflammation caused by breathing in certain allergens.
is allergic asthma (IgE-mediated) triggered by common environmental allergens.
is a heart muscle problem caused by diseases outside the heart.
is kidney inflammation that can cause blood in urine and swelling.
is a genetic eye disorder causing abnormal retinal vessels and vision loss.
is a rare inherited eye disorder affecting retinal blood vessels and vision.