RS761656636 EFEMP2

Health Risk Chr 11:65870545
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Associated Conditions
Cutis laxa
autosomal recessive
type 1B
Familial aortopathy
Cutis laxa
autosomal recessive
type 1B
Familial aortopathy
Other Variants in EFEMP2
rs119489101 rs119489102 rs193302865 rs193302868 rs193302867 rs193302869 rs193302870 rs193302864 rs193302866 rs397514683
Ask Dr. Hemsworth about this variant