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 cancer of the rectum, causing bleeding and bowel changes.
is an early rectal cancer limited to the innermost lining.
is a rare cancer in the rectum's blood and lymph vessels.
is a rare cancer of the rectum's smooth muscle tissue.
is a rare cancer that starts in the rectum's lymphatic tissue.
is a rare, aggressive cancer that begins in pigment-producing cells.
is a rectal cancer that makes mucus and starts in gland cells.
is a rare tumor in the rectum from hormone-producing cells.
is a rare cancer of muscle-forming cells in the rectum.
is a rare cancer that starts in tissues of the rectum.
is a rare, aggressive rectal cancer with both epithelial and sarcoma-like cells.
is a rare, aggressive rectal cancer with mucus-producing signet ring cells.
is a rare cancer arising from squamous cells in the rectum.
causes repeated painful breakdown of the cornea’s outer surface.
causes repeated hepatitis C-related liver disease after a liver transplant.
is a rare disorder causing repeated episodes of extreme sleepiness.
is a recurring eye inflammation causing optic nerve swelling and vision changes.
is a rare immune disorder causing repeated infections from abnormal white cells.
is an immune disorder causing repeated infections due to missing antibody types.
is a rare inherited disorder causing metabolic crises, rhabdomyolysis, and arrhythmias.
is an inherited immune disorder causing repeated serious Neisseria bacterial infections.
is a rare HPV-related condition causing wart-like growths in the airways.
is a rare genetic muscle disorder causing progressive weakness and muscle wasting.
is a rare genetic muscle disease causing progressive weakness and disability.