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 genetic condition affecting multiple body systems, including the kidneys.
is a rare genetic disorder causing widespread body effects and primary lymphedema.
is a condition where pressure on the optic nerve affects vision.
are rare inherited disorders affecting how the body processes certain sugars.
are conditions that disrupt vitamin D processing, affecting bones and calcium balance.
is when the upper stomach pushes through the diaphragm opening.
is a chronic inflammatory scalp condition causing painful lumps, drainage, and scarring.
is widespread inflammation of the retina and choroid that can affect vision.
is a rare inflammatory connective-tissue disorder involving eosinophils and multiple tissues.
is a serious condition causing widespread blood clotting and bleeding.
is a rare condition causing benign smooth muscle growths in the abdomen.
is a sun-related skin condition causing many dry, scaly ringlike spots.
is a condition causing memory loss, usually after stress or trauma.
involves disconnection between thoughts, identity, memory, feelings, or surroundings.
is a rare genetic condition that can affect development, learning, and behavior.
is a rare genetic condition affecting development, learning, and sometimes behavior.
is a rare genetic condition caused by missing DNA on chromosome 17.
is a rare genetic condition that can affect development and health.
is a rare genetic condition caused by extra DNA on chromosome 22.
is a rare genetic condition that can affect development and learning.
is an inherited muscle disease that mainly weakens the lower legs.
is a genetic condition causing joint stiffness mainly in hands and feet.
is a rare inherited condition causing permanently bent fingers and toes.