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 brainstem cancer in adults with rapidly worsening symptoms.
is a rare brainstem tumor with mixed glial cells in adults.
is a rare, aggressive brain or spinal cord cancer from pregnancy-related cells.
is a rare, fast-growing brain or spinal cord cancer in adults.
is a rare central nervous system germ cell tumor, highly treatable.
is a rare adult brain or spinal cord germ cell tumor.
is a rare, typically benign brain or spinal cord germ cell tumor.
is a rare brain or spinal tumor combining multiple germ cell types.
is a rare brain or spinal cord germ cell tumor, sometimes cancerous.
is a cerebellar brain tumor in adults causing balance and coordination problems.
is a rare malignant brain tumor from cerebrospinal fluid–producing tissue.
is a rare, benign kidney tumor with cysts, often cured surgically.
is a usually benign tumor containing mature tissues, often ovarian.
is an autoimmune disease causing muscle weakness and a distinctive skin rash.
is a rare, aggressive brain tumor marked by chromosome 19 changes (C19MC).
is an adult, fast-growing germ cell cancer of ovaries or testes.
is a rare soft tissue cancer that often spreads to lymph nodes.
is a rare soft-tissue cancer (sarcoma) forming bone-like tissue outside bones.
is a rare soft tissue sarcoma outside bones, often in limbs.
is a rare adult-onset inherited disorder causing kidney failure and spastic quadriparesis.
is a rare soft-tissue cancer starting in connective tissue cells.
is a primary liver cancer in adults, often from chronic liver disease.
is a rare genetic disorder causing fragile bones, pain, and dental issues.