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 serious condition where abnormal fluid builds up in a fetus.
is an enlarged gallbladder filled with mucus, usually from duct blockage.
is a rare genetic disorder causing severe anemia, acidosis, and organ failure.
is a rare inherited metabolic condition affecting tryptophan breakdown.
is a tapeworm infection of the intestines, often causing mild symptoms.
is a rare inherited immune disorder causing recurrent infections and eczema.
is a rare inherited immune disorder causing repeated infections and high IgE.
is a rare immune disorder causing eczema, repeated infections, and high IgE.
is a rare immune disorder causing frequent infections and low antibody switching.
is a rare inherited metabolic disorder with high beta-alanine levels.
is a rare immune disorder causing eczema and repeated infections.
is a rare inherited immune disorder with recurrent infections and abnormal antibodies.
is a rare inherited immune disorder causing recurrent infections and weak immunity.
is a rare inherited immune disorder causing frequent infections and abnormal antibodies.
is a rare immune disorder causing low antibodies and repeated infections.
is a rare immune disorder causing severe, recurrent, and opportunistic infections.
is a genetic immune disorder: high IgM, low others, no opportunistic infections.
is an inherited condition with unusually high HDL (good) cholesterol levels.
is an inherited condition causing unusually high HDL ("good") cholesterol levels.
is a rare inherited disorder causing dangerous ammonia buildup in blood.
is a rare genetic disorder causing dangerous ammonia buildup and brain problems.
causes higher-than-normal male-type hormones, leading to symptoms like acne or excess hair.
is a rare inherited disorder causing excess androgen hormones and related symptoms.
is a rare inherited disorder causing high arginine and nervous system problems.