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 cancer caused by genetic changes in blood-forming or lymphatic tissues.
is an inherited birth difference affecting the urinary and reproductive organs.
is a genetic condition causing tumors in the urinary and reproductive organs.
is an inherited tendency to develop recurring hives and sometimes swelling.
is a group of inherited blood vessel disorders that vary widely.
is an inherited disorder affecting liver, bile duct, pancreas, or spleen development.
is a common sexually transmitted infection that causes recurring genital sores.
is a rare genetic syndrome affecting the genitals, palate, heart, and development.
is a rare genetic disorder causing joint, genital, and developmental problems.
is a rare genetic disorder causing multiple cartilage growths near bones.
is a rare genetic bone disorder causing multiple benign cartilage growths.
is a harmless condition causing smooth, patchy areas on the tongue.
is a rare fungal infection caused by Geotrichum species.
is a noncancerous tumor that develops from reproductive cells.
is a tumor starting in cells that normally become eggs or sperm.
is a testicular cancer arising from germ cells, usually highly treatable.
is a rare genetic condition that affects development and body growth.
is a rare, usually treatable tumor arising from germ cells.
is a rare brain or spinal cord tumor arising from germ cells.
is a rare genetic disorder with loose skin and osteoporosis.
is a brain disorder affecting writing, math, finger recognition, and left-right orientation.
is a rare inherited prion disease causing worsening coordination and dementia.
is a rare pregnancy-related cancer that usually responds well to treatment.
is high blood sugar during pregnancy that can affect parent and baby.