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 bone disorder causing short stature and skeletal changes.
is a rare genetic bone disorder causing short stature and loose joints.
is a rare genetic disorder affecting bone growth and joint stability.
is a rare genetic bone disorder causing short stature and flexible joints.
is a rare genetic disorder affecting bone growth, joints, spine, and teeth.
is a rare genetic disorder affecting bone growth and causing sparse hair.
is a rare genetic bone disorder causing short limbs and abnormal calcification.
is an inherited bone growth disorder causing short stature and joint problems.
is a rare genetic bone disorder affecting growth, joints, and spine.
is a rare genetic bone disorder affecting growth, spine, and joints.
is a rare genetic skeletal disorder affecting bone growth and joint shape.
is a rare inherited disorder affecting bone growth, spine, and joints.
is a rare inherited bone disorder affecting growth, spine, and joints.
is a rare genetic condition affecting bone growth, joints, and spine.
is a rare genetic skeletal disorder affecting spine and bone growth.
is a rare genetic bone disorder causing short stature and spine-limb abnormalities.
is a genetic bone disorder affecting spine growth, joints, and height.
are rare genetic bone disorders that affect spine, joint, and bone growth.
is a rare genetic skeletal disorder causing short stature and joint problems.