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 an immune disorder with low antibodies and recurrent infections.
is a genetic immune disorder causing low antibodies and recurrent infections.
is a genetic immune disorder with low antibodies and recurrent infections.
is a primary immune disorder with low antibodies, recurrent infections, autoimmunity.
is an inherited immune disorder with low antibodies, recurrent infections, and autoimmunity.
is a harmless skin growth from human papillomavirus (HPV) infection.
is a rare birth defect linking airway and esophagus, causing complications.
is buildup of brain fluid, from poor absorption, enlarging ventricles.
involves persistent difficulties with speech, language, or social communication skills.
is dangerous pressure buildup in muscles reducing blood flow, requiring emergency treatment.
is overexpansion of healthier lung areas after nearby tissue loss, helping breathing.
is a rare immune disorder causing recurrent severe bacterial infections, sometimes autoimmunity.
is a rare inherited complement protein deficiency causing recurrent meningococcal infections.
is an immune disorder causing recurrent infections and autoimmune complications.
is a complement system disorder causing recurrent bacterial infections and autoimmunity.
is a rare genetic disorder causing complement overactivation, thrombosis, and protein-losing enteropathy.
is a genetic condition where XY individuals can't respond to male hormones.
is a birth heart defect with holes and one atrioventricular valve.
is a complex congenital heart defect with central hole and underdeveloped ventricle.
is a congenital heart defect affecting central walls and valves, requiring surgery.
is a rare congenital heart defect combining AVSD and tetralogy of Fallot.
is a rare birth condition with fused eyelids and vision loss.
is a rare disorder causing near-total body fat loss and metabolic complications.