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 COL4A1-related disorder affecting vessels, kidneys, eyes, brain, muscles.
is a common skin condition causing dry, itchy, irritated hands.
is a rare genetic condition affecting hand, foot, urinary, and genital development.
is a common viral illness causing mouth sores and a hand-foot rash.
is a rare viral illness causing fever, bleeding, and kidney problems.
is a rare viral disease from rodents causing sudden, severe lung failure.
is a rare genetic condition affecting development, learning, behavior, and speech.
is a rare genetic syndrome affecting development, behavior, learning, and growth.
is a rare genetic condition affecting development, behavior, and sometimes growth.
is a rare cancer that starts in the roof of the mouth.
is a rare genetic skin disorder causing very thick, tight skin.
is a rare nerve disorder causing one-sided facial flushing and sweating.
is a very rare genetic disorder with features that can vary.
is a rare inherited disorder affecting how the body absorbs tryptophan.
is a rare genetic condition affecting brain, limb, and facial development.
is a rare bacterial infection causing fever, rash, and joint pain.
is a rare inherited tyrosine-metabolism disorder causing infant feeding problems and acidosis.
is a severe alpha thalassemia causing life-threatening fetal anemia and swelling.
is a rare, aggressive blood cancer related to hairy cell leukemia.
is a group of cancers affecting the mouth, throat, nose, or sinuses.
is a cancer that starts in the mouth, throat, or nearby tissues.
is an inherited condition causing hearing loss and reduced aldosterone response.
is a bulging, weakened area of the heart wall or nearby vessel.
is a rare cancer that starts in or spreads to the heart.