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 inherited birth-onset muscle disease causing weakness and low tone (hypotonia).
is a genetic muscle disorder causing early low tone, weakness, and delays.
is a rare inherited muscle disease present from birth, causing weakness.
is a rare inherited muscle disorder causing weakness from birth; severity varies.
is a genetic muscle disorder present from birth causing weakness and hypotonia.
is a rare inherited muscle disorder causing early weakness and low tone.
is a rare inherited muscle disorder from birth causing weakness and hypotonia.
is a rare inherited muscle disease causing weakness and hypotonia from birth.
is a genetic muscle disorder causing hypotonia and weakness from birth.
is a genetic muscle disorder causing early-onset weakness and low muscle tone.
causes lifelong, inherited muscle weakness from birth, with severity varying widely.
is a rare inherited muscle disease causing lifelong weakness from birth.
is a genetic muscle disorder present from birth causing lifelong muscle weakness.
is a rare inherited muscle disorder causing early hypotonia and weakness.
is a rare inherited muscle disorder causing early-life muscle weakness.
is a genetic muscle disorder causing early-onset weakness and structural cores.
is a rare genetic muscle disorder present from birth, causing weakness.
is a genetic muscle disorder from birth with weakness and myasthenic-like fatigability.
is a congenital muscle disorder from fewer type 2 fibers, causing weakness.
is a genetic muscle disorder causing weakness and low muscle tone (hypotonia).
is a genetic muscle condition causing stiffness and delayed relaxation (myotonia).
is a genetic muscle disorder causing weakness at birth and breathing difficulties.