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 testicular tumor causing painless swelling; sometimes producing estrogen.
is a rare vaginal soft-tissue cancer from immature muscle cells in adults.
is a rare benign skin disorder causing yellow-orange nodules, usually solitary.
is a late-onset condition causing coordination problems (ataxia) and widespread nerve damage.
is a rare inherited white-matter disease causing progressive movement and thinking problems.
is an autosomal recessive, adult-onset disorder causing progressive coordination and balance problems.
is a rare genetic anemia starting in adulthood with ring sideroblasts.
is a genetic movement disorder causing involuntary neck contractions and abnormal postures.
is a mitochondrial disorder causing progressive eye muscle weakness and ptosis.
is a genetic muscle disorder from VCP mutations, causing adult distal weakness.
is a movement disorder causing dystonia and parkinsonism (Parkinson-like symptoms) in adults.
is a retinal disease causing gradual central vision loss and distortion.
is a rare adult immune disorder causing severe infections, especially nontuberculous mycobacteria.
is a rare mitochondrial disease causing progressive muscle weakness and fatigue.
is an autoimmune disease causing fluctuating muscle weakness, worse with activity.
is a late-onset muscle disease causing progressive weakness and breathing problems.
is chronic airway inflammation starting in adulthood, with frequent, hard-to-control symptoms.
is a genetic, multisystem condition causing muscle weakness, myotonia, and fatigue.
is a rare inflammatory disorder causing high fevers, rash, and joint pain.
is a rare autoinflammatory disease causing high fevers, rash, joint pain.
is a urea cycle disorder causing high ammonia (hyperammonemia) and neuropsychiatric crises.
is a circadian rhythm disorder causing very early sleep and wake.
is a circadian rhythm disorder causing unusually early sleep and wake times.
is a circadian rhythm disorder causing very early sleep-wake timing, often genetic.