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 pancreatic cancer that often makes thick mucus-producing tumors.
is a usually benign mucus-producing cyst in the pancreatic ducts.
is a mucus-producing pancreatic cyst that can sometimes become cancer.
is a pancreatic cancer that develops from a mucus-producing duct tumor.
is a rare pancreatic cancer that starts in mucus-producing cysts.
is a usually noncancerous, mucus-filled cystic tumor of the pancreas.
is a pancreas condition causing mucus buildup and widening of ducts.
is a rare pancreatic neuroendocrine tumor that does not cause hormone symptoms.
is a noninvasive pancreatic cyst growth that can become cancerous.
is a mucus-producing pancreatic cyst tumor that has not invaded nearby tissue.
is a rare cancerous cystic tumor of the pancreas.
is a usually noncancerous pancreatic cyst made of fluid-filled sacs.
is a usually noncancerous pancreatic cystic tumor that often causes no symptoms.
is a rare, aggressive pancreatic cancer with signet ring-shaped cells.
is a rare pancreatic tumor that often grows slowly and is treatable.
is a rare pancreatic tumor that makes excess somatostatin hormone.
is a rare, aggressive pancreatic cancer made of squamous cells.
causes greasy, foul-smelling stools when the pancreas cannot digest fat.
is a rare digestive disorder that causes trouble absorbing dietary fats.
is a rare pancreatic tumor that causes severe watery diarrhea.
is a rare pancreatic cancer that usually affects children.
is a shortage of all blood cells causing fatigue, infections, bleeding.
is a rare genetic disorder causing low levels of all blood cells.
is a rare genetic disorder causing low blood cells and developmental delays.