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 skin condition causing thickened skin on the palms and soles.
is a lung cancer near the lung top that can affect nerves.
is a condition affecting the pancreas, sometimes disrupting digestion and blood sugar.
is a rare cancer that starts in the pancreas’s lymphatic tissue.
is a rare cancer that starts in the pancreas's connective tissues.
is a rare pancreatic cancer that starts in enzyme-producing cells.
is a rare tumor that makes ACTH and causes Cushing syndrome.
is a deadly cancer starting in the pancreas, often diagnosed late.
is a rare, aggressive pancreatic cancer with glandular and squamous cell features.
is a rare genetic disorder affecting pancreas and early brain development.
is a pancreatic cancer that often develops silently and spreads early.
causes severe watery diarrhea and salt loss from a rare hormone-secreting tumor.
is a rare inherited condition causing poor fat digestion and diarrhea.
is a rare, usually slow-growing cystic tumor of the pancreas.
is a rare pancreatic cancer that forms cystic, mucus-producing tumors.
is a usually benign cystic tumor that forms in the pancreas.
is a rare pancreatic tumor arising from hormone-making delta cells.
is an aggressive pancreatic cancer starting in ducts, often diagnosed late.
is the most common type of pancreatic cancer, often diagnosed late.
is a rare, aggressive cancer that starts in the pancreas's hormone-making cells.
is a rare type of pancreatic cancer with mucus-producing tumor cells.
is a rare tumor that makes too much gastrin, causing ulcers.
is a rare genetic syndrome causing pancreatic underdevelopment, diabetes, and heart defects.
is a rare inherited disorder causing poor digestion, anemia, and bone thickening.