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 an immune reaction to wheat that can cause mild to severe symptoms.
is a rare immune disorder causing infections, warts, and low white cells.
is a rare bacterial infection that can affect digestion, joints, and brain.
is a harmless skin condition causing small white bumps on the neck.
is a rare genetic condition causing a white forelock and birth differences.
is a rare genetic condition affecting brain development, movement, and learning.
is a mild fungal infection causing white nodules on hair shafts.
is a rare inherited platelet disorder causing large, pale platelets and bleeding.
is an allergic reaction to white shrimp, causing symptoms after eating.
is a rare, harmless inherited condition causing white, spongy mouth patches.
is a rare inherited condition causing white, spongy patches in the mouth.
is a rare inherited condition causing harmless white, spongy mouth patches.
is a rare genetic condition affecting development, learning, speech, and behavior.
is a rare rodent-borne viral illness that can cause severe fever.
is a highly contagious bacterial infection that causes severe coughing fits.
is a very rare genetic disorder causing aging-like features from birth.
is a rare genetic condition affecting growth, development, and learning.
is a rare amyloid buildup disorder that can affect joints and bones.
is a protein buildup disorder affecting the heart, nerves, and tendons.
is an age-related protein buildup that can affect the heart and nerves.
is a syndrome with fused neck bones, hearing loss, and eye problems.
is a genetic condition affecting development, learning, behavior, and heart health.
is a genetic condition affecting development, learning, behavior, and the heart.
is a rare lung disorder causing weak airways, bronchiectasis, and breathing problems.