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 tumor in the gland that stores and releases hormones.
is a cataract at the back of the lens affecting vision.
is a rare inherited corneal disorder affecting endothelium, sometimes causing blurry vision.
is an inherited corneal disorder that can cause blurred vision and glaucoma.
is an inherited eye disorder affecting the cornea, sometimes causing vision problems.
is a rare inherited corneal disorder that can blur vision.
is painful inflammation in the back of the eye.
is a rare cancer in the tube carrying urine from the bladder.
is a birth defect blocking urine flow from the bladder.
is a rare eye cancer that starts in the back uvea.
is inflammation at the back of the eye that can threaten vision.
is a rare genetic brain development disorder causing severe neurologic problems.
is a heart attack affecting the heart's lower back walls.
is a type of heart attack affecting the heart's back and side.
is a group of digestive problems that can happen after stomach surgery.
is a slow-growing blood and lymph node cancer of mature B cells.
is an autoimmune movement disorder causing involuntary movements after some infections.
is brain inflammation after infection that affects balance and coordination.
is brain inflammation that develops after an infection and affects brain function.
is inflammation of blood vessels that develops after an infection.
is lung scarring that can develop after inflammation or serious infection.
is thinning and dryness of vaginal tissues after menopause.
is a rare genetic syndrome causing small head size, weakness, and delays.