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 genetic disorder causing bone overgrowth and short stature.
is a rare genetic disorder causing severe insulin resistance and growth problems.
is a chronic bacterial infection affecting skin, nerves, and sometimes eyes.
is a chronic infection affecting skin, nerves, and eyes; curable with antibiotics.
is a rare cancer of the membranes around brain and spinal cord.
is a bacterial infection usually spread through water contaminated by animal urine.
is a rare genetic disorder affecting bones, joints, and growth.
is a genetic growth disorder causing short stature and wrist deformity.
is a rare inherited disorder affecting purine metabolism, movement, and behavior.
causes pain, weakness, or numbness along the leg and foot.
is a rare inherited skin disorder causing severe blistering and life-threatening complications.
is a rare inherited disorder causing severe, often life-threatening artery weakness.
is an inherited disorder causing ataxia, deafness, vision loss, and early death.
is a severe condition causing life-threatening brain and heart birth defects.
is a severe genetic bone disorder that is usually fatal before birth.
is a rare inherited disorder causing severe joint contractures before birth.
is a rare inherited disorder causing severe joint stiffness before birth.
is a rare genetic disorder causing severe facial, heart, and limb abnormalities.
is a rare inherited condition causing severe brain, kidney, and gut defects.
is a rare genetic condition causing severe brain, kidney, and genital underdevelopment.
is a rare genetic condition causing severe anemia and genital differences.