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 bleeding disorder caused by too little factor VII.
is a rare bleeding disorder causing easy bruising and prolonged bleeding.
is a rare bleeding disorder from low factor XI, often post-surgery.
is a rare bleeding disorder caused by missing clotting factor XIII.
is a rare inherited immune disorder causing severe infections and inflammation.
is a rare cancer starting in the tubes between ovaries and uterus.
is a rare, usually benign tumor of the fallopian tube.
is a rare, benign tumor of the fallopian tube lining.
is a very rare cancer of the fallopian tube's connective tissue.
is a noncancerous growth in the fallopian tube.
is a rare, aggressive cancer of the fallopian tube with mixed cells.
is a rare cancer that starts in a fallopian tube lining.
is a rare, usually benign growth in the fallopian tube.
is a condition affecting the tubes that carry eggs to the uterus.
is a rare cancer starting in the fallopian tube lining.
is endometriosis affecting the fallopian tubes, often causing pelvic pain.
is a rare cancer starting in germ cells of the fallopian tube.
is a rare pregnancy-related cancer that starts in the fallopian tube.
is a rare, noncancerous smooth muscle tumor in the fallopian tube.
is a rare cancer of the fallopian tube’s smooth muscle.
is a rare cancer in the mucus-making lining of the fallopian tube.
is a rare growth in the fallopian tube that makes mucus.
is a rare cancer that starts in a fallopian tube.