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 hole in the intestine that can cause a serious infection.
is an inherited condition causing many intestinal polyps and higher cancer risk.
is a rare tuberculosis infection that affects the intestines and nearby tissues.
is a rare cervical cancer subtype with mucus-producing, intestine-like cells.
is a twisting of the intestine that can block digestion and blood flow.
is an early-stage cancer limited to the intestine’s inner lining.
is a rare cancer of mast cells in abdominal lymph nodes.
is a rare brain tumor with a fluid-filled cyst nearby.
is a serious brain infection causing a pocket of pus.
is a weak, bulging brain artery that can leak or rupture.
is narrowing of brain arteries that can reduce blood flow.
is hardening of brain arteries that can reduce blood flow.
is a bulging brain blood vessel that can leak or burst.
is a bulging weak spot in a brain blood vessel.
is an inherited disorder causing weak, bulging spots in brain arteries.
is a bulging brain blood vessel that can leak or rupture.
is an inherited condition causing weak brain blood vessels and aneurysms.
is an inherited blood vessel weakness that can cause brain aneurysms.
is a bulging brain blood vessel that may rupture and bleed.
is a weakened brain blood vessel that can bulge or rupture.