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 inherited skin condition causing soft, sagging patches.
is an inherited condition causing multiple painful fatty lumps under the skin.
is an inherited condition that weakens the aorta and raises tear risk.
is an inherited disorder causing very high triglycerides and pancreatitis risk.
is a rare genetic condition causing very high triglycerides and pancreatitis.
is an inherited condition causing unusually flexible joints and related symptoms.
is an inherited tendency to irregular heartbeat (atrial fibrillation), raising stroke risk.
is an inherited condition causing benign tumors in the heart's upper chambers.
is an inherited heart rhythm disorder causing atrial arrhythmias and slow conduction.
is an inherited disorder causing numerous atypical moles and high melanoma risk.
is an inherited hip disorder causing bone death from poor blood flow.
is a rare inherited disorder causing recurrent mouth, genital, and skin ulcers.
is an inherited skin condition causing recurring painful blisters and raw patches.
is an inherited condition causing low copper levels, usually without serious illness.
is an inherited retinal condition with harmless flecks, usually without vision problems.
is an inherited condition where the aortic valve has two flaps.
is an inherited joint condition causing calcium crystal buildup and arthritis.
is a rare inherited condition affecting development of the lower spine.
is an inherited eye condition affecting the optic nerve and vision.
is an inherited condition causing fragile blood vessel clusters in the brain.
is an inherited tendency to develop balloon-like brain artery bulges.
is an inherited tendency for neck artery tears that can cause stroke.
is a rare inherited lupus causing painful cold-triggered skin sores.
is a rare inherited blood disorder that can resemble chronic leukemia.