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 inflammation of connective tissue that causes pain and stiffness.
is a parasitic liver infection usually caused by contaminated water plants.
is a rare parasitic infection that mainly affects the liver.
is a parasitic intestinal infection caused by a large fluke worm.
is a rare inherited mitochondrial disease causing severe infant brain dysfunction.
is a harmless breast condition caused by damaged fatty tissue.
is a severe inherited heart muscle disease linked to abnormal glycogen buildup.
is a rare inherited brain disease causing worsening insomnia and early death.
is a rare inherited mitochondrial disorder causing severe symptoms in infancy.
is a rare inherited muscle disorder causing severe stiffness and early death.
is a rare inherited metabolic disorder causing severe illness in infancy.
is a severe inherited mitochondrial disorder that disrupts the body's energy production.
is a rare, severe brain disorder that worsens after some viral infections.
is a rare birth condition affecting leg, foot, and sometimes hand development.
is a rare inherited disorder causing worsening movement, vision, and nerve problems.
is a rare inherited disorder affecting energy use, heart function, and ketones.
is a rare inherited disorder affecting fat use and enlarging heart muscle.
is a rare genetic condition affecting brain, vision, and development.
is a reaction in G6PD deficiency that can destroy red blood cells.
is a rare inherited nerve disorder causing worsening face and throat weakness.
is a rare genetic condition causing developmental delay, brain differences, and syndactyly.
is a rare epilepsy syndrome triggered by a fever-related illness.
is a rare genetic condition affecting fingers, toes, head growth, and development.
is a rare genetic condition affecting fingers, toes, head size, and development.