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 tumor in the upper throat present at birth.
is a common infection causing a runny nose, sore throat, and sneezing.
is a rare inherited disorder causing bone cysts and early dementia.
is a rare genetic disorder affecting growth, development, and sexual maturation.
is a rare genetic muscle condition with weakness and anesthesia complications.
is a rare inherited disorder affecting the nerves, liver, and development.
is a genetic heart muscle disease causing arrhythmias, woolly hair, thickened palms/soles.
is a rare genetic brain disorder causing severe microcephaly and developmental delay.
is a severe asthma attack that can quickly become life-threatening.
is a hookworm infection that can cause anemia and stomach symptoms.
is a rare skin condition causing shiny patches usually on the shins.
is a rare chronic skin disease causing yellow plaques near the eyes.
is death of a tiny middle ear bone, affecting hearing.
is death of pituitary tissue that can disrupt hormone production.
is a rare eye cancer that can damage vision and spread.
is a serious intestinal disease that mainly affects premature babies.
is a rare, fast-spreading soft tissue infection needing urgent treatment.
is a rare, life-threatening stomach infection that causes tissue death.
is a rare, usually harmless condition causing a sore on the palate.
is a rapidly spreading, life-threatening infection that destroys skin and deeper tissues.
is a rare genetic disorder causing severe skeletal abnormalities before birth.
is a rare condition causing ACTH-producing pituitary tumor growth after adrenal removal.
is a rare genetic disorder causing muscle weakness and breathing problems.
is a genetic muscle disorder causing weakness, breathing problems, and delayed movement.