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 genetic condition affecting head size, fingers, toes, and learning.
is a rare rheumatoid arthritis complication with low white blood cells.
is a rare rheumatoid arthritis complication causing infections and an enlarged spleen.
is a breast cancer that begins in tissue extending into the armpit.
is a common cancer that starts in breast tissue, mainly in women.
is breast cancer that starts in the milk ducts or lobules.
is a cancer that starts in the central part of the breast.
is breast cancer in the lower inner area of the breast.
is breast cancer located in the lower outer part of the breast.
is a rare breast cancer affecting the nipple and surrounding areola.
is breast cancer that begins in the upper inner breast area.
is a breast cancer that starts in the upper outer breast.
is an inherited cause of infertility where embryos cannot implant normally.
causes infertility because egg cells cannot mature properly for fertilization.
is infertility caused by an abnormal egg outer layer (zona pellucida).
is infertility caused by problems with the uterus affecting pregnancy.
is a cancer that starts in the lining of female reproductive organs.
is a noncancerous growth in the female reproductive organs.
is a cancer that starts in the female reproductive organs.
affects the ovaries, uterus, or related organs and tissues.
is a rare genetic epilepsy affecting females, often with learning difficulties.
is urine leakage during activities that put pressure on the bladder.
is a rare cancer that starts in the tube carrying urine.
is a rare genetic condition affecting development, learning, and other body systems.