RS193302866 EFEMP2

Health Risk Chr 11:65868557
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What This Variant Does
"CLNSIG=5
Associated Conditions
Cutis laxa
autosomal recessive
type 1A
type 1B
Cutis laxa
autosomal recessive
type 1A
type 1B
Other Variants in EFEMP2
rs119489101 rs119489102 rs193302865 rs193302868 rs193302867 rs193302869 rs193302870 rs193302864 rs397514683 rs572394429
Ask Dr. Hemsworth about this variant