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 genetic disorder causing poor growth and adrenal problems.
is a rare gallstone complication that blocks or compresses the bile duct.
is a brain-related condition causing confusion between reflections and real objects.
is a rare genetic disorder with mirror polydactyly and spinal-limb defects.
is a rare birth difference causing symmetrical extra fingers or toes.
is a genetic brain disorder causing abnormal movements and progressive nerve damage.
is a movement problem caused by progressive damage to the brain.
is a rare kidney cancer linked to changes involving the TFE genes.
is a rare disorder with variable symptoms and severity across individuals.
is a skin condition caused by tiny mites living on people.
is an inherited condition that raises melanoma and kidney cancer risk.
is a rare inherited disorder that reduces cells' ability to make energy.
is a rare inherited mitochondrial disorder that reduces cells' energy production.
is a rare inherited disorder impairing mitochondrial energy production, causing multisystem symptoms.
is a rare genetic disorder that impairs cellular energy production.
is a rare inherited disorder that impairs energy production in cells.
is a rare genetic disorder that reduces cellular energy production.
is a rare mitochondrial disorder causing energy failure, muscle weakness, developmental delays.
is a genetic mitochondrial disorder that reduces cells' ability to make energy.