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 condition causing swollen tear and salivary glands.
is a rare inherited brain disorder with milder developmental and movement problems.
causes noticeable thinking and memory changes beyond normal aging.
is a mild bleeding disorder caused by low factor VIII levels.
is a mild bleeding disorder caused by low factor IX levels.
is an inherited condition causing mildly high phenylalanine levels in the blood.
is a milder inherited condition where the body poorly breaks down phenylalanine.
is an inherited disorder that can cause excess uric acid buildup.
is a pregnancy complication causing high blood pressure and mild organ stress.
is a genetic bone condition causing short stature and early arthritis.
is a heat rash caused by blocked sweat glands or ducts.
is a harmless heat rash causing tiny clear sweat-blister bumps.
is a heat rash caused by blocked sweat glands deep in skin.
is a heat rash causing small pus-filled bumps in blocked sweat glands.
is a serious form of tuberculosis that spreads throughout the body.
is an immune reaction to milk proteins that can cause symptoms.
is a skin infection from cattle that causes small hand nodules.
is a rare disorder causing eye weakness, poor coordination, and reflex loss.
is a rare movement disorder causing slowly worsening stiffness and weakness.
is a genetic condition causing lifelong leg swelling (lymphedema) from birth.
is a group of disorders affecting the body's balance of minerals.
is an inherited condition causing minimal pigment and vision problems.
is a rare, usually benign growth in the vulvar vestibular glands.
is a rare genetic disorder affecting bone growth, joints, and height.