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, present-at-birth fluid-filled sac in the pancreas.
is a rare, benign skin lesion present from birth involving hair follicles.
is a rare birth defect missing part of the heart sac.
is a congenital heart defect where some lung veins connect incorrectly.
is present at birth; kneecap (patella) remains dislocated, causing knee instability.
is a rare bulge (aneurysm) of the ductus arteriosus.
is a birth defect affecting the heart’s protective sac (pericardium).
is a rare inherited bleeding disorder causing poor clot stabilization and hemorrhage.
is a rare birth defect where blood from intestines bypasses the liver.
is a rare inherited blood disorder causing prolonged clotting tests without bleeding.
is a rare birth condition where the eye lens is absent.
is a rare inherited disorder causing chronic limb swelling from lymphatic malformation.
is a lymphatic disorder present at birth causing limb swelling only.
is a birth defect with enlarged ureter causing urine flow blockage.
is a congenital condition of enlarged ureter without reflux or obstruction.
is a birth defect causing enlarged ureter and urine outflow blockage.
is a birth defect causing enlarged ureter with urine backflow and blockage.
is a birth defect causing enlarged ureter from urine backflow (reflux).
is a rare genetic disorder causing marrow failure, weak immunity, skeletal abnormalities.
is a rare congenital condition where the collarbone doesn’t fully fuse.
is a rare birth condition causing thighbone weakness, bowing, and nonhealing fractures.
is a rare condition present at birth where fibula fails to unite.
is a rare birth condition causing fragile bones and false joints.
is a rare birth condition where the forearm bone (radius) doesn’t unite.