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 eye disease causing gradual vision loss over time.
is an inherited eye disorder causing gradual vision loss over time.
is an inherited eye disorder that causes gradual vision loss.
is an inherited eye disorder causing night blindness and gradual vision loss.
is an inherited retinal disease causing night blindness and progressive vision loss.
is an inherited eye disorder that gradually causes worsening vision loss.
is an inherited eye disorder that causes progressive vision loss.
is an inherited eye disease that gradually reduces night and side vision.
is a genetic retinal disorder causing progressive night blindness and tunnel vision.
is an inherited eye disorder causing gradual night and side-vision loss.
is an inherited eye disease that gradually causes worsening vision loss.
is an inherited eye disorder causing progressive vision loss.
is an inherited eye disorder that gradually causes vision loss.
is an inherited eye disorder causing gradually worsening vision loss.
is an inherited eye disorder causing gradual night and peripheral vision loss.
is an inherited retinal disorder causing gradual night and side vision loss.
is an inherited eye disorder causing night blindness and progressive vision loss.
is an inherited retinal disease causing progressive night blindness and tunnel vision.
