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 fungal corneal infection that can cause pain and vision loss.
is a rare birth defect affecting spinal cord and back development.
is inflammation of the spinal cord that can cause weakness and numbness.
is a rare spinal birth defect where the spinal cord protrudes.
is a group of bone marrow disorders causing faulty blood cell production.
is a bone marrow disorder causing anemia and abnormal blood cells.
is a rare blood cancer causing abnormal, overproduced blood cells.
is a rare blood cancer with abnormal blood cell production.
is a blood cancer causing marrow scarring, anemia, and spleen enlargement.
is a rare, aggressive blood cancer driven by FGFR1 gene fusions.
is a rare blood cancer driven by an abnormal PDGFRA gene change.
is a rare blood cancer driven by PDGFRB gene rearrangements.
is a group of blood cancers with high eosinophils and gene changes.
is a blood disorder affecting bone marrow and myeloid blood cells.
is a blood and bone marrow cancer affecting myeloid cells.
is a leukemia affecting some children with Down syndrome.
is a cancer of blood-forming cells in the bone marrow.
is a rare cancerous tumor of immature blood cells outside bone marrow.
is a rare blood cancer caused by changes involving the FGFR1 gene.
is a rare blood cancer caused by an abnormal JAK2 gene fusion.
is a rare blood cancer caused by a PDGFRA gene rearrangement.
is a rare blood cancer driven by PDGFRB gene changes.
are rare blood cancers with high eosinophils caused by certain gene changes.
is a birth defect where the spinal cord does not develop normally.