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 muscle disorder causing weakness and delayed motor development.
is a genetic bone disorder causing overly dense, fragile bones.
is a rare inherited disorder affecting the brain, nerves, and development.
is inflammation in the middle eye, often causing floaters and blurred vision.
is a mild form of asthma with symptoms that come and go.
is leg pain during walking caused by reduced blood flow.
is a mental health condition causing sudden repeated episodes of impulsive anger.
causes repeated episodes of joint swelling, usually without lasting damage.
is a rare inherited disorder causing harmful amino acid buildup.
is occasional bulging of an eye, often from pressure behind it.
is an eye condition where one eye sometimes turns out of alignment.
is a rare nerve tumor made of immature and mature cells.
is a rare, noncancerous fatty growth in the inner ear canal.
is a usually benign tumor near the hearing and balance nerves.
is a rare birth condition where one internal carotid artery is missing.
are swollen veins inside the rectum that can cause painless bleeding.
is an eyelid stye caused by an infected or blocked oil gland.
is a rare process where tooth structure is lost from within.
is an eye movement disorder causing trouble coordinating both eyes.
is a chronic bladder condition causing pain, pressure, and frequent urination.
is a rare inflammatory condition causing skin rash and joint pain.
is inflammation of the cornea that can cause pain and blurred vision.
is a group of disorders causing lung scarring and breathing problems.
is a rare genetic disease causing lung scarring and breathing difficulties.