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 gallbladder cancer made of fast-growing neuroendocrine cells.
is a rare, aggressive gallbladder cancer that often spreads before diagnosis.
is a rare genetic disorder affecting brain development and kidney function.
is a rare genetic disorder causing brain abnormalities and kidney disease.
is a rare genetic disorder causing kidney problems and developmental delays.
is a rare genetic disorder affecting brain development, kidneys, and growth.
is a rare genetic condition affecting brain development and kidney function.
is a rare inherited condition affecting brain development and often the kidneys.
is a rare blood cancer caused by abnormal gamma heavy-chain proteins.
is a rare inherited disorder affecting brain signaling and development.
is a rare inherited disorder affecting brain development and movement.
is a rare inherited disorder affecting glutathione metabolism and antioxidant protection.
is a rare blood cancer involving abnormal antibody heavy chain proteins.
is a genetic muscle disease causing progressive hip and shoulder weakness.
is a rare inherited disorder causing episodes of muscle weakness or paralysis.
is a rare genetic condition that can affect development and health.
is a rare, usually noncancerous tumor made of mature nerve cells.
is a rare brain tumor made of nerve and support cells.
is a noncancerous, fluid-filled lump near a joint or tendon.
is a rare nerve tissue tumor that can be benign or cancerous.
is a rare, usually benign nerve tumor that often causes few symptoms.
is a rare inherited disorder where harmful fats build up in cells.
is a genetic disorder causing growth delay, hair loss, and dental problems.
is an inherited condition causing colon polyps and increased cancer risk.