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 condition causing absent nails from birth.
is a lifelong inability to smell that is present from birth.
is a rare birth difference affecting the tiny hearing bones.
is a rare condition with underdeveloped or absent breast tissue.
is painless, birth-present enlargement of fingertips and toes without other disease.
is a rare birth condition where the eyelid turns outward.
is a rare eyelid condition where the lid turns inward at birth.
is a rare inherited liver disorder causing scarring and portal hypertension.
is a rare birth condition where the tongue is unusually small.
is a rare birth condition with an underdeveloped or absent tongue.
is a rare birth condition causing delayed or absent puberty and infertility.
is a rare inherited condition with unusually large corneas from birth.
is a condition where a baby’s head is unusually small at birth.
is a rare birth condition causing narrowed nasal passages and breathing trouble.
is a rare birth condition causing underdeveloped or missing fingernails.
is a birth difference where part of the elbow joint is displaced.
is a rare birth condition causing cloudy, hardened corneas.
is a rare birth condition where the upper and lower jaws fuse.
is a rare birth defect where the heart's major arteries are reversed.
is an inherited condition causing lifelong low platelet counts without other problems.
is a birth difference where the brain's connecting bridge is absent.
is a rare birth condition where skin covers partially formed eyes.
is a rare inherited disorder that reduces cells’ ability to make energy.
is a rare brain malformation affecting the cerebellum and fluid spaces.