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 muscle disease that causes progressive weakness.
is epilepsy where specific triggers, like flashing lights, provoke seizures.
is a chronic pain condition causing severe limb pain, swelling, and sensitivity.
is reduced vision caused by untreated focusing problems during early childhood.
is a common focusing problem causing blurred vision at any distance.
is a bone marrow disorder causing too few healthy red blood cells.
is a blood disorder causing low blood counts and excess immature cells.
is a serious blood disorder with abnormal marrow cells and leukemia risk.
is a myelodysplastic syndrome causing anemia and increased immature blood cells.
is a high-risk myelodysplastic syndrome with excess immature blood cells.
is celiac disease that continues despite a strict gluten-free diet.
is a bone marrow disorder causing low levels of multiple blood cells.
is a rare blood cancer that does not respond to treatment.
is a blood cancer that does not respond to treatment.
is a rare blood cancer that resists standard treatment.
is a hard-to-treat blood and lymph system cancer of T cells.
is a rare inherited disorder causing phytanic acid buildup and nerve damage.
is a rare tooth development disorder causing weak, poorly formed teeth.
is a cancer that starts in the tube carrying urine.
is a rare form of Guillain-Barré syndrome affecting specific nerve areas.
is a rare genetic bone disorder causing short stature and spine changes.
causes blurred vision because the eye focuses light unevenly.
is an inherited eye disorder that causes recurrent corneal erosions and scarring.
is a rare brain or spinal cord tumor linked to RELA fusion.