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 inherited nerve disorder causing progressive balance and coordination problems.
is a rare X-linked bone growth disorder causing short stature and deformities.
is a rare inherited bone disorder causing short stature and joint problems.
is an inherited bleeding disorder causing low platelets despite normal platelet size.
is a rare inherited blood-clotting disorder linked to changes in F9.
is a rare inherited condition causing multiple birth differences in several organs.
is an inherited condition causing unusually strong responses to warfarin.
is a rare inherited enzyme disorder causing excess xanthine and kidney stones.
is a rare genetic disorder causing low uric acid and xanthine stones.
is a rare, severe gallbladder inflammation that can resemble cancer.
is a rare, severe kidney infection that can destroy kidney tissue.
is a rare disorder causing yellow-brown skin bumps and sometimes diabetes insipidus.
is a rare inherited disorder causing fatty deposits and other health problems.
is dry, rough eyelid skin that may cause irritation and discomfort.
is a rare genetic disorder causing extreme UV sensitivity and skin cancers.
is a rare inherited disorder causing extreme sunlight sensitivity and skin cancer.
is a rare inherited DNA-repair disorder with extreme UV sensitivity, skin cancers.
is a rare inherited disorder causing extreme sunlight sensitivity and skin cancers.
is a rare inherited disorder causing extreme sensitivity to sunlight and cancers.
is a rare inherited disorder causing extreme sensitivity to ultraviolet light.
is a rare inherited disorder linked to sun sensitivity and skin cancers.
is a rare inherited disorder causing extreme sun sensitivity and skin cancers.