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 heart muscle disease that enlarges and weakens the heart.
is an inherited heart condition that weakens and enlarges the heart.
is an inherited disorder causing heart enlargement, weak pumping, and arrhythmias.
is an inherited heart muscle disease that enlarges and weakens the heart.
is an inherited dilated cardiomyopathy causing enlarged ventricles and reduced pumping.
is an inherited heart muscle disease causing an enlarged, weakened heart.
is an inherited cardiomyopathy with enlarged, weakened ventricles and heart failure.
is genetic heart muscle disease with enlarged ventricles and reduced output.
is an inherited heart disease causing enlarged, weak chambers and poor pumping.
is an inherited heart condition that weakens and enlarges the heart muscle.
is a genetic heart-muscle disease causing enlarged, weakened ventricles and heart failure.
is an inherited heart muscle disease causing enlargement, weak pumping, and arrhythmias.
is an inherited heart muscle disease causing enlarged ventricles and heart failure.
is a genetic heart disease causing enlarged ventricles, arrhythmias, and heart failure.
is an inherited heart muscle disease causing dilation, weak pumping, and arrhythmias.
is an inherited heart condition that enlarges and weakens the heart.
is an inherited heart muscle disease that weakens and enlarges the heart.
is an inherited heart muscle disease that weakens the heart's pumping.
