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 disorder causing abnormal heart valve development and leakage.
is a rare genetic condition causing short stature, delayed speech, developmental differences.
is a benign jaw condition where bone is replaced by dense tissue.
is a rare genetic condition that can affect several body systems.
is an intense fear of flying that can cause severe anxiety.
is a rare inherited disorder affecting nerves, hearing, and movement.
is a rare inherited skin condition causing small thickened bumps.
is inflammation in the retina and choroid that can affect vision.
is a rare genetic disorder affecting the skin, limbs, eyes, and face.
causes involuntary muscle contractions that affect one specific body area.
is kidney inflammation caused by infected clots blocking small blood vessels.
is a seizure disorder starting in one brain area, sometimes spreading.
is a rare genetic disorder causing seizures, learning problems, and brain malformations.
is a rare, harmless HPV-related condition causing small bumps in the mouth.
is a rare genetic condition affecting facial skin development before birth.
is a rare genetic condition causing abnormal facial skin development.
is a rare genetic condition affecting facial skin and nearby features.
is a movement disorder causing involuntary hand muscle contractions during specific tasks.
is inner ear inflammation that can cause sudden dizziness and hearing changes.
is a rare inflammatory muscle condition causing a localized painful swelling.
is an inherited skin condition causing thickened skin on palms and soles.
is a rare inherited disorder causing thickened skin on palms and soles.