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 red cell disorder causing anemia, jaundice, and enlarged spleen.
is a genetic red cell disorder causing anemia, jaundice, and enlarged spleen.
is an inherited red blood cell disorder causing anemia and jaundice.
is an inherited red blood cell disorder causing hemolytic anemia and jaundice.
is an inherited blood disorder causing fragile, sphere-shaped red blood cells.
is a rare inherited red blood cell disorder that can cause anemia.
is an inherited nerve disorder triggered or worsened by heat exposure.
is an inherited disorder causing low platelets and early bone marrow scarring.
is an inherited low platelet count with normal-sized platelets and bleeding risk.
is an inherited blood-clotting disorder caused by too little antithrombin.
is a rare inherited clotting disorder increasing risk of abnormal blood clots.
is an inherited condition that increases the risk of Wilms tumor.
is a rare inherited disorder that can cause xanthine kidney stones.
is an inherited disorder causing high blood pressure in lung arteries.
is a rare genetic disorder causing albinism, bleeding, and lung disease.
is a rare genetic condition causing albinism, bleeding issues, and lung disease.
is a rare genetic disorder causing albinism, easy bleeding, and immune problems.
is a rare inherited disorder affecting pigment, bleeding, and sometimes lungs.
is a rare inherited disorder causing albinism, bleeding, and sometimes lung disease.
is a rare inherited disorder affecting pigmentation, bleeding, and sometimes immunity.
is a rare inherited disorder affecting pigmentation, bleeding, and cell function.
is a rare inherited disorder affecting pigment, bleeding, and immune function.
is a rare inherited disorder causing albinism, easy bleeding, and vision problems.