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 problem with the heart's electrical system controlling heartbeat.
is a rare syndrome causing heart defects and extra fingers or toes.
is a rare genetic condition causing heart defects and shortened limbs.
is a group of conditions affecting the heart and blood vessels.
is a rare cancer that starts in the heart's fibrous tissue.
is a rare cancer that starts in the heart's smooth muscle.
is a rare, usually noncancerous fatty growth in or around the heart.
is a rare cancer that starts in the heart’s tissues.
is a rare cancerous tumor of blood vessel cells in the heart.
is a condition where the heart sits in an unusual position.
is a rare cancer that starts in the heart's tissues.
is a hole in the heart wall present at birth.
is damage or dysfunction of one or more heart valves.
is a rare genetic condition affecting the heart and hand development.
is a rare inherited condition affecting heart rhythm and hand development.
is a rare inherited condition affecting the heart and hand development.
is a rare inherited disorder causing heart defects and hand differences.
is a rare disorder where abnormal proteins build up in organs.
is a rare immune system cancer involving abnormal antibody heavy chains.
is a rare genetic condition that can affect growth and development.
is a bony growth on the heel that can cause pain.
is a rare genetic disorder causing hearing loss and tooth enamel defects.
is an inherited condition causing hearing loss, enamel defects, and vision problems.
is a rare cow's milk allergy causing lung problems and anemia.