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 inherited disorder affecting bones, growth, and cornea clarity.
is a rare genetic bone disorder causing short stature and spinal curvature.
is a rare genetic bone disorder affecting the spine and long bones.
is a rare genetic disorder affecting bone growth, joints, and stature.
is a rare genetic bone disorder causing short stature and skeletal changes.
is a rare bone disorder causing short stature and bowed legs.
is a rare inherited bone disorder affecting growth, joints, and breathing.
is a rare genetic disorder affecting bone growth, stature, and limbs.
is age-related spine wear causing pain, stiffness, and nerve compression.
is an itchy, inflamed skin rash often linked to eczema.
is a hole in the intestine that develops without a clear cause.
is a spinal fluid leak causing headaches that worsen when upright.
is a rare disorder causing repeated episodes of unusually low body temperature.
is a life-threatening collapsed lung that traps air and impairs breathing.
is a rare disorder causing worsening balance, coordination, and speech problems.
is the most common type of breast cancer, occurring without inherited risk.
is a rare rapidly progressive brain disease caused by abnormal prion proteins.
is a rare prion disease causing worsening insomnia and brain decline.
is a rare condition where the developing brain is damaged before birth.
is a rare prion brain disease causing rapidly progressive neurological decline.
causes an exaggerated startle response and sudden muscle stiffness.
is a rare childhood brain disorder affecting movement and development.
is a usually noninherited tumor that makes excess stress hormones.
is a liver-related disorder causing light-sensitive skin blistering and fragility.