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 heart rhythm disorder causing dangerously fast, abnormal heartbeats.
is an inherited heart rhythm disorder affecting the heart's natural pacemaker.
is an inherited condition causing recurrent lung collapse (spontaneous pneumothorax).
is a rare inherited disorder causing kidney protein loss and adrenal failure.
is a genetic disorder causing steroid-resistant nephrotic syndrome and sensorineural hearing loss.
is an inherited trait causing one or more extra nipples.
is an inherited condition causing fluid-filled cavities in the spinal cord.
is an inherited seizure disorder affecting the temporal lobes of the brain.
is an inherited disorder causing enlargement and tearing of the chest aorta.
is an inherited disorder causing high platelet counts and clotting risk.
are inherited changes affecting blood clot control, sometimes increasing bleeding or clotting.
is an inherited neck cyst that forms from leftover fetal tissue.
is an inherited disorder where the thyroid cannot make hormones properly.
is a rare inherited disorder causing calcium deposits around joints.
is an inherited condition where urine flows backward from bladder to kidneys.
is an inherited disorder affecting digestive and urinary tract smooth muscles.
is a rare inherited cancer that starts in the fallopian tubes.
is an inherited ovarian cancer that runs in some families.
is a genetic condition causing bone marrow failure and increased cancer risk.
is a rare inherited disorder that can cause bone marrow failure.
is a rare inherited disorder causing bone marrow failure and cancer risk.
is a rare inherited DNA-repair disorder causing bone marrow failure and cancers.
is a rare inherited DNA-repair disorder causing bone marrow failure, cancers.
is a rare inherited Fanconi anemia subtype causing marrow failure and cancers.