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 cancer that starts in the pancreas.
is a rare cancer that starts in the small intestine.
is a rare stomach cancer that starts in the stomach lining.
is a rare heart disease that can affect how the heart works.
causes uncommon abnormal heartbeats that may lead to fainting or sudden death.
is an uncommon growth in the heart that may affect function.
is a group of uncommon heart muscle diseases that affect pumping.
is a rare cause of high blood pressure.
is a rare disease affecting blood vessels in the brain and retina.
is early puberty caused by premature activation of brain hormone signals.
is when puberty starts unusually early because brain signals begin too soon.
is an uncommon dementia caused by reduced blood flow damaging the brain.
causes involuntary, dance-like movements that can affect daily life.
is a rare eye disorder affecting the choroid, the layer beneath retina.
is a genetic condition from chromosome changes, causing varied health and development.
is a group of uncommon blood vessel or circulation disorders.
is a group of uncommon bleeding disorders that affect blood clotting.
is a rare disorder causing abnormal blood vessel growth in multiple tissues.
is a rare heart birth defect affecting the wall between ventricles.
is a rare heart defect present at birth without other syndromic features.
is an uncommon eye infection causing redness, irritation, and discharge.
is a rare inherited anemia present from birth.
is an inherited bone marrow disorder causing low blood cell counts.
is a rare inherited anemia that causes ongoing red blood cell breakdown.