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.
affects how the body absorbs and moves sugars from food.
is a group of conditions affecting how the body processes carbohydrates.
is a group of inherited disorders affecting how the body uses fats.
is a rare inherited disorder affecting the body’s stress hormone production.
is a group of inherited disorders affecting vitamin B12 use and transport.
is an inherited condition that causes harmful copper buildup in the body.
is a group of conditions affecting how the body makes energy.
is a rare inherited disorder affecting fat breakdown and ketone production.
is a group of inherited conditions affecting how the body uses fat.
is a rare genetic disorder affecting how the body uses folate.
is an inherited condition that affects how the body processes fructose.
is a rare inherited disorder affecting fucose-containing sugar production and body function.
is an inherited disorder affecting how the body processes galactose, a sugar.
is a rare inherited condition affecting how the body breaks down GABA.
is a rare inherited condition that disrupts how the body uses glutamine.
is a rare inherited disorder affecting how the body processes glycerol.
is a rare inherited condition affecting how the body breaks down sugar.
is a rare inherited condition affecting cell-surface sugar molecules and development.
is a rare inherited condition causing harmful oxalate buildup, often in kidneys.
is a rare inherited condition affecting how the body breaks down histidine.
is an inherited condition affecting how the body moves and uses iron.
is a rare inherited disorder that prevents the body using ketones.
is a rare metabolic condition that affects the body's use of ketones.
is a rare inherited condition that impairs fat absorption and transport.