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 rectal cancer that starts in flat lining cells.
is a rare small bowel cancer arising from the intestine’s lining cells.
is a rare stomach cancer that starts in flat lining cells.
is a growth of abnormal squamous cells that may become cancer.
is a harmless, wart-like skin growth caused by overgrowth of cells.
is a usually harmless wart-like growth caused by human papillomavirus (HPV).
is a rare inherited disorder that affects development and body systems.
is a rare inherited disorder affecting protein processing, development, and learning.
is a mosquito-borne viral infection that can cause brain inflammation.
is an aggressive blood cancer affecting B cells in lymph nodes.
is an eye condition that causes a cone-shaped, thinning cornea.
is a rare genetic condition causing developmental delays, distinctive features, and reflux.
is a genetic condition causing hearing loss and broad thumbs and toes.
is a severe staph lung infection that can rapidly damage tissue.
is a bacterial skin infection causing painful blistering and peeling skin.
is a staph bacterial skin infection causing fever, rash, and peeling.
is a toxin-related illness caused by toxins made by staph bacteria.
is a serious bacterial illness causing fever, rash, low blood pressure, and shock.
is a foodborne illness caused by toxins made by Staphylococcus bacteria.
is an outward bulging of the back of the eye.
is an inherited eye disease that causes progressive central vision loss.
is a rare epilepsy causing seizures triggered by sudden unexpected stimuli.
is a rare inherited immune disorder causing early autoimmune problems across organs.
is a severe asthma attack that does not improve with usual treatment.