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 common skin condition causing inflamed, sometimes itchy or painful hair follicles.
is a rare type of skin lymphoma affecting hair follicles.
is an immune overreaction to foods, causing hives, swelling, anaphylaxis (life-threatening emergency).
is a rare but serious illness caused by toxin-contaminated food.
is a usually slow-growing tumor near the brainstem and upper spinal cord.
is a rare visual processing disorder causing trouble recognizing shapes and forms.
is a skin reaction caused by allergy to formaldehyde exposure.
is a rare metabolic disorder affecting folate use and histidine breakdown.
is a rare genetic condition affecting development, hearing, and learning.
is a rare birth defect affecting structures in the lower neck.
is an eye movement problem causing vertical double vision and head tilt.
is a rare genetic eye condition affecting vision and early eye development.
is a rare inherited eye disorder causing underdeveloped fovea and early cataracts.
is a rare cause of urinary retention from abnormal sphincter relaxation.
is a rare inherited blood vessel disorder that can affect the brain.
is a rare skin condition causing itchy bumps in sweat gland areas.
is a rare genetic brain disorder affecting development, movement, speech, and learning.
is a rare genetic brain development disorder causing severe developmental delays.
is an inherited condition causing developmental delay, learning challenges, and autism-like behaviors.
is an inherited condition causing early loss of normal ovarian function.
is a genetic neurologic condition causing tremor, balance problems, and thinking changes.
is a rare inherited disorder affecting bones, eyes, heart, and facial development.
is a rare genetic condition affecting development before birth.