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 disorder causing shortened metacarpal and metatarsal bones.
is a genetic condition causing shortened hand and foot bones.
is a rare genetic condition causing short fingers/toes and early severe hypertension.
is a congenital genetic condition causing short fingers and elbow-wrist deformities.
is a rare genetic condition causing short fingers/toes with unusually long thumbs.
is a rare genetic disorder affecting limb growth, learning, and heart development.
is a genetic disorder with short fingers, nystagmus (eye jerks), and ataxia.
is a rare genetic condition causing short fingers and inward great toes.
is a genetic syndrome with short fingers, short stature, and vision loss.
is a genetic, present-at-birth condition causing short and fused fingers and toes.
is a rare, inherited birth condition with short, fused fingers/toes.
is a rare genetic condition causing short stature, nail and bone abnormalities.
is a rare genetic bone condition causing short trunk and spine problems.
is a rare genetic disorder causing short-trunk stature and fragile tooth enamel.
is a genetic skeletal condition causing short trunk, flattened vertebrae, and scoliosis.
is a rare genetic skeletal disorder causing stippled cartilage and short fingertips.
is a rare genetic condition causing short fingertips, facial differences, delayed puberty.
is a rare genetic condition that affects early body development.
causes slow vision, trouble with moving objects, and delayed light adjustment.
is a rare inherited retinal condition causing slow vision after light changes.
is a rare inherited retinal disorder causing delayed vision after light changes.
is an abnormal cluster of brain blood vessels that can bleed.
is a rare genetic disorder with abnormal brain calcium deposits causing symptoms.
is cancer in the brain, forming tumors affecting thinking, movement, body functions.