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 condition affecting development, growth, and distinctive physical features.
is a rare breast cancer affecting the nipple and nearby skin.
is a chronic condition with abnormal bone remodeling, causing enlarged, fragile bones.
is an inherited disorder that disrupts bone remodeling and weakens bones.
is a rare inherited disorder that causes abnormal bone breakdown and regrowth.
is an inherited bone disorder that weakens normal bone remodeling.
is a rare inherited disorder causing enlarged, weak, and misshapen bones.
is a rare genetic condition that affects development and body systems.
is a rare birth condition affecting facial development and sometimes the brain.
is a rare genetic disorder affecting purine production and brain development.
is a rare brain condition causing reduced awareness or recognition of pain.
is a condition causing ongoing pain that affects daily life.
is a rare movement disorder causing leg pain and involuntary toe movements.
is a rare genetic disorder causing painful nerve tumors and Marfan-like features.
is a genetic condition affecting the palate, teeth, facial features, and development.
is a type of inflammatory arthritis causing sudden, repeated joint attacks.
is a skin reaction caused by allergy to palladium in metal items.
is a rare genetic condition causing brain growths, extra digits, hormonal problems.
is a rare inherited disorder causing thickened palms/soles and hearing loss.
is an inherited condition with thick palms/soles and high esophageal cancer risk.
is a rare inherited disorder causing thickened palms, soles, and nerve damage.
is a rare inherited disorder causing thickened palms, soles, and leg stiffness.
is a genetic syndrome with thick palms, sex reversal, and SCC risk.
is an inherited skin condition causing thickened palms and soles.