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 lung disease causing scarring and breathing problems.
is a group of lung diseases causing inflammation, scarring, and breathing problems.
is a group of adult lung diseases causing scarring and breathing problems.
is a group of rare childhood lung diseases that affect breathing.
is a rare group of infant lung disorders affecting breathing.
is a rare genetic condition affecting the lungs, kidneys, and skin.
is inflammation of the heart muscle that can affect pumping.
is kidney inflammation that can reduce kidney function.
is a glaucoma type caused by occasional blockage of eye drainage.
is a bulging of the wall between the heart’s lower chambers.
is a birth defect where part of the intestine is blocked.
is a noncancerous growth in the intestines that may need monitoring.
is a rare illness where gut bacteria make toxin causing weakness.
is when the intestines lack enzymes needed to digest certain sugars.
is a broad term for disorders affecting the intestines and digestion.
is a digestive disorder where poor fat absorption causes diarrhea and weight loss.
is a digestive disorder caused by abnormal absorption of certain vitamins.
is a severe blockage of stool in the intestines or rectum.
is an infection of the intestines that often causes diarrhea and cramping.
is a rare disorder where intestinal lymph vessels leak protein.
is a birth defect where the intestines do not form normally.
is a rare, usually noncancerous tumor arising from hormone-making intestinal cells.
is a blockage in the intestines that prevents food and fluid passing.
is a rare inherited condition causing bowel blockage in newborn babies.