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 an autosomal-dominant condition causing isolated, often progressive sensorineural hearing loss.
is an autosomal-dominant, non-syndromic sensorineural hearing loss, often progressive, with variable onset.
causes isolated hearing loss without other health problems; dominantly inherited.
causes isolated hearing loss, typically passed down in families (dominant).
is inherited (autosomal dominant), non-syndromic hearing loss, often progressive.
is inherited, usually progressive inner-ear hearing loss without other symptoms.
is a genetic, autosomal dominant inner-ear (sensorineural) hearing loss without other features.
is genetic, autosomal dominant inner ear hearing loss without other issues.
is an inherited hearing loss (sensorineural), autosomal dominant, without other features.
is an inherited condition causing progressive inner-ear hearing loss and balance problems.
is a rare genetic bone disorder causing short arms, legs, and stature.
is a genetic optic nerve condition causing gradual childhood vision loss.
is an inherited eye disorder causing optic nerve damage, cataracts, vision loss.
is an inherited disorder causing progressive vision loss and peripheral neuropathy.
is a hereditary condition causing vision loss, hearing loss, and muscle weakness.
is an inherited optic nerve disorder causing progressive childhood-onset vision loss.
is a genetic disorder with overly dense bones and possible nerve compression.
is a rare inherited skeletal disorder causing hearing loss and joint-spine abnormalities.
is a genetic condition causing thickened palms/soles and congenital hair loss.
is an inherited disorder causing multiple kidney cysts and gradual kidney failure.
is a rare genetic disorder causing kidney cysts and tuberous sclerosis features.
is an inherited disorder causing knee webbing, clefts, and limb differences.
is an autosomal-dominant disorder causing extra thumbs/toes (preaxial polydactyly) and upper-back hypertrichosis.
is a rare inherited kidney disorder causing low blood magnesium and hypocalciuria.