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 inherited lysosomal disorder causing progressive brain and behavior decline.
is a rare inherited disorder causing low calcium, growth problems, and delays.
is a rare inflammatory disorder affecting bones, joints, and skin.
is a parasitic infection that can affect muscles, intestines, or both.
is inflammation of the brain and spinal cord lining caused by sarcoidosis.
is an inflammatory condition causing tiny clumps (granulomas) in multiple organs.
is a cancer that starts in bone or soft tissues.
is a rare cervical cancer that starts in the cervix's connective tissues.
is a rare cancer of the uterus's muscle or supporting tissues.
is a rare form of basal cell skin cancer.
is a rare, aggressive cancer with both epithelial and sarcoma-like cells.
is a rare, aggressive cancer usually affecting the lining of the lungs.
is a rare, aggressive penile cancer with spindle-shaped squamous cells.
is a rare, aggressive kidney cancer that can spread quickly.
is a rare, aggressive form of squamous cell skin cancer.
is a rare, aggressive bladder cancer with both epithelial and sarcoma-like cells.
is a rare, aggressive uterine lining cancer with mixed tumor cells.
is a rare condition involving multiple cancerous tumors in connective tissues.
is a rare cancer affecting the membranes around the brain and spine.
is a rare, aggressive bile duct cancer that starts inside the liver.
is a rare inherited condition with high sarcosine levels, often harmless.
is a rare genetic condition causing developmental delays, especially with speech.
is a rare genetic disorder causing developmental delay and significant speech problems.
is a genetic condition causing developmental delay, speech impairment, and dental differences.