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 kidney cancer that begins in the kidney’s filtering tubes.
is a cancer that usually starts in glandular tissue, often ovaries.
is a rare squamous cell cancer with finger-like, wartlike growths.
is a rare cancer of the thymus gland with papillary features.
is a common bladder cancer that starts in the urinary tract lining.
is a rare brain tumor arising near the pineal gland.
is a usually benign wart-like growth caused by human papillomavirus.
is a rare benign brain tumor causing excess cerebrospinal fluid and hydrocephalus.
is a rare inherited disorder causing severe gum disease and thickened palms.
is a rare, harmless skin condition causing small, firm bumps.
is a rare harmless skin condition causing small waxy bumps in children.
is a rare, harmless skin condition causing small yellowish bumps.
is an acetaminophen overdose that can seriously damage the liver.
is a very rare soft tissue tumor that usually grows slowly.
is a rare birth defect affecting the heart's tricuspid valve.
is a fungal infection mainly in Latin America that often affects lungs.
is a rare tumor from nerve tissue, sometimes producing excess hormones.
is a parasitic infection linked to eating raw freshwater crab or crayfish.
is a rare condition causing facial weakness or paralysis from birth.
is a temporary intestinal blockage that stops food and gas moving.
is a rare viral illness that can cause permanent muscle weakness.
is an eye misalignment caused by weakness or paralysis of eye muscles.
is a rare birth defect causing a facial cleft near the midline.
is a rare birth difference causing a split in the nose’s center.