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 disorder with severe facial and limb differences.
is a rare genetic condition affecting facial features, limbs, and tooth development.
is a rare genetic disorder causing facial, nasal, and limb differences.
is a rare genetic disorder causing thin, fragile, prematurely aged skin.
is a skin condition causing thickened, rough palms and soles.
is a rare inherited skin disorder causing small palm and sole bumps.
is a rare genetic skin condition causing wart-like bumps on hands/feet.
is a rare inherited skin disorder causing wart-like bumps on extremities.
is a hormonal disorder in adults causing enlarged hands, feet, face.
is a rare skin disorder causing dark patches on hands and feet.
is a rare genetic bone disorder causing short limbs and short stature.
is a rare congenital condition causing facial, limb, and brain malformations.
is a rare genetic skeletal disorder causing short limbs and height.
is a rare genetic bone disorder causing limb shortening and short stature.
is a rare genetic skeletal condition with limb shortening and short stature.
is a rare inherited skeletal condition causing severe limb and digit shortening.
is a rare inherited skeletal dysplasia causing limb shortening and short stature.
is a rare inherited bone disorder causing short stature and limb shortening.
is a rare genetic bone disorder causing short stature, short hands/feet.
is a rare genetic disorder causing bone loss, keloids, and early aging.
is a rare genetic condition affecting development of limbs, ears, and eyes.
is a rare genetic condition affecting hand, foot, and chest development.
is a rare genetic skeletal disorder affecting hands, feet, chest, and spine.
is a rare genetic condition causing limb malformations and kidney anomalies.