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 birth difference causing a split in the lip or palate.
is an inherited brain disorder causing behavior, language, and thinking changes.
is an inherited condition affecting the food pipe and stomach.
is an inherited kidney disorder that affects the glomeruli, the kidneys' filters.
is an inherited cancer affecting the ovaries, uterus, or other reproductive organs.
is a genetic condition that affects hair growth, texture, or structure.
is a genetic condition causing head and neck malformations before birth.
is an inherited blood disorder affecting hemoglobin, the protein that carries oxygen.
is a rare inherited disorder causing kidney injury, anemia, and low platelets.
is an inherited disorder causing excess aldosterone and early high blood pressure.
is an inherited condition causing high ferritin levels without excess body iron.
is an inherited condition causing overactive parathyroid glands and high calcium.
is an inherited condition causing darker patches or overall skin pigmentation.
is a rare inherited condition causing low calcium from underactive parathyroid glands.
is an inherited condition causing lighter-than-usual skin, hair, or eyes.
is an inherited immune disorder that can also affect the skin.
is when genetic changes affect fertility in women, men, or both.
is a rare inherited joint disease causing inflammation, pain, and stiffness.
is a group of inherited lung disorders causing scarring and breathing problems.
is an inherited disorder affecting the intestines and how they function.
is a genetic intestinal disease that causes poor absorption of fats.
is an inherited condition causing many intestinal polyps and increased cancer risk.
is a rare inherited disorder causing severe, hard-to-control diarrhea in infancy.
is a rare inherited condition affecting the voice box and breathing.