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 disorder causing bone marrow failure and cancer risk.
is a genetic Fanconi anemia subtype with bone marrow failure.
is a rare inherited DNA-repair disorder causing bone marrow failure and cancers.
is a rare inherited disorder that impairs DNA repair and bone marrow.
is a rare inherited DNA repair disorder causing marrow failure and cancers.
is a rare inherited Fanconi anemia subtype with bone marrow failure.
is a rare inherited disorder that can cause bone marrow failure.
is a rare genetic Fanconi anemia subtype with marrow failure, cancer risk.
is a rare proximal tubule disorder causing urinary nutrient and bicarbonate losses.
is a rare genetic kidney disorder causing nutrient wasting and acidosis.
is an inherited kidney tubule disorder causing excess nutrient loss in urine.
is a rare inherited kidney disorder that leaks vital nutrients into urine.
is a rare inherited kidney disorder causing mineral loss and weak bones.
is a rare inherited disorder affecting sugar use, growth, liver, and kidneys.
is a kidney tubule disorder causing loss of nutrients into urine.
is a tick-borne bacterial infection that causes fever, rash, and illness.
is a rare genetic lysosomal storage disease causing painful nodules and arthritis.
is a rare inherited disorder causing painful joint swelling and nodules.
is an allergic lung disease caused by breathing in moldy dust.