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, noncancerous pleural tumor that may cause chest symptoms.
is a rare, noncancerous prostate growth that may recur locally.
causes repeated bile flow blockage (cholestasis), triggering intense itching and jaundice.
is a rare genetic liver disorder causing recurring bile-flow blockages and jaundice.
is a rare inherited liver disorder causing recurring itching and jaundice.
is high blood pressure caused by narrowed kidney arteries, often manageable.
is a rare inherited muscle disorder present at birth causing mild weakness.
is a slow-growing, noncancerous nerve sheath tumor causing pain or numbness.
is high blood pressure from an identifiable cause, usually treatable.
are brief, harmless shivering episodes in young children, not epileptic seizures.
is a noncancerous germ cell tumor containing varied tissues, often ovarian/testicular.
is a noncancerous growth in the tubes connecting ovaries to uterus.
is an extremely rare, noncancerous vaginal tumor with mixed tissue types.
is a noncancerous growth of blood vessels, forming lumps or birthmarks.
is a rare genetic immune disorder with chronic B-cell overgrowth and infections.
is an immune skin reaction to benzisothiazolinone exposure, causing itchy rash.
is allergic contact dermatitis (skin allergy) to benzoic acid preservatives.
is a drug allergy to benzylpenicillin (penicillin G) causing hives, swelling, anaphylaxis.
is caused by thiamine (vitamin B1) deficiency, affecting nerves and heart.
is a rare inherited platelet disorder causing easy bruising and bleeding.
is a rare inherited platelet disorder causing mucocutaneous bleeding and macrothrombocytopenia.
is an occupational lung disease from beryllium exposure causing lung inflammation.
is an inherited eye disease causing gradual central vision loss from childhood.
is sexual activity with animals, associated with legal, ethical, and health risks.