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, aggressive prostate cancer arising from squamous cells.
is a rare cancer that starts in the prostate's supportive tissues.
is a rare prostate cancer arising from cells lining the urinary tract.
is the most common type of prostate cancer, arising in gland cells.
is a noncancerous enlargement of prostate tissue that can affect urination.
is a fluid-filled sac in or near the prostate gland.
is an enlarged prostate that can cause urinary symptoms in aging men.
is a rare bladder-type cancer arising in the prostate's urinary channel.
is a rare cancer in the urethra near the prostate.
is prostate inflammation that can cause pelvic pain and urination problems.
is inflammation of the prostate and bladder causing urinary symptoms and pain.
is a rare inherited inflammatory disease causing recurrent fevers, rash, and pain.
is a rare inherited autoinflammatory disease with fevers, rash, lipodystrophy.
is a rare genetic autoinflammatory disorder causing recurrent fevers, rash, and inflammation.
is a condition that raises the risk of abnormal blood clots.
is an inherited blood clotting disorder that raises abnormal clot risk.
is anemia caused by too little protein to make healthy red blood cells.
causes too much protein to leak from the intestines.
is excess protein in the urine, often signaling kidney problems.
is a rare genetic inflammatory disorder causing recurrent fever and skin rashes.
is a rare inherited inflammatory disease causing recurrent fevers and skin symptoms.
is a rare disorder causing uneven overgrowth of bones, skin, and tissues.
is a rare disorder causing uneven overgrowth and other body changes.