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 autoimmune disease causing lifelong insulin deficiency and high blood sugar.
is an autoimmune disease where the body stops making insulin.
is a condition where the body stops making insulin.
is an autoimmune disease where the pancreas stops making insulin.
is an autoimmune disease causing lifelong insulin dependence and high blood sugar.
is a long-term autoimmune disease that stops the body making insulin.
is an autoimmune disease causing high blood sugar from too little insulin.
is a lifelong autoimmune condition where the body stops making insulin.
is a lifelong condition where the body makes little or no insulin.
is a rare inherited form of diabetes caused by insulin gene changes.
is a rare inherited diabetes caused by a change in one gene.
is an autoimmune disease causing insulin deficiency, requiring lifelong insulin therapy.
is an autoimmune condition where the body stops making insulin.
is a rare immune disorder caused by too much type I interferon.
is a rare childhood immune disorder causing excess inflammation throughout the body.
is a rare, usually noncancerous kidney tumor found in kidney tubules.
is a genetic condition affecting connective tissue, bones, joints, hearing, and vision.