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 inherited heart rhythm disorder that can cause dangerous arrhythmias.
is a genetic heart rhythm disorder increasing risk of fainting and arrhythmias.
is a genetic subtype causing dangerous heart rhythm (arrhythmia), often during sleep.
is a rare inherited heart rhythm disorder causing dangerous arrhythmias and fainting.
is an inherited heart rhythm disorder with prolonged QT and dangerous arrhythmias.
is an inherited heart rhythm disorder that can trigger dangerous arrhythmias.
is a rare inherited heart rhythm disorder that can cause dangerous arrhythmias.
is a birth difference where part of an arm or leg underdevelops.
is a congenital tissue wall dividing the vagina lengthwise, sometimes causing symptoms.
is a hair growth disorder causing easily pulled, slow-growing scalp hair.
is a tick-borne viral disease that mainly affects sheep.
is a bacterial infection spread by body lice, causing repeated fever episodes.
is a bladder problem where pressure stays high as it fills.
is a slow-growing brain tumor that can affect thinking and function.
is when the placenta sits low in the uterus during pregnancy.
is an inherited kidney disorder causing proteinuria, high urine calcium, and nephrocalcinosis.
is a genetic liver condition causing recurrent gallstones from low bile phospholipids.
is an eye condition that damages the optic nerve despite normal pressure.
is a prolonged, painful erection caused by trapped blood in the penis.
is a slow-growing brain tumor that may affect thinking, movement, or seizures.
is a rare, slow-growing cancer arising from hormone-producing uterine cells.
is a rare inherited disorder affecting the eyes, brain, and kidneys.
is a usually slow-growing tumor near the lower skull base.
is a rare mouth cancer affecting the lower gums and nearby tissues.