RS200133966 ELN

Health Risk Chr 7:74063191
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Associated Conditions
Cutis laxa
autosomal dominant 1
Supravalvar aortic stenosis
Inborn genetic diseases
Cutis laxa
autosomal dominant 1
Supravalvar aortic stenosis
Inborn genetic diseases
Other Variants in ELN
rs137854452 rs2486324663 rs2132322943 rs1797225811 rs2486562061 rs1563826213 rs137854454 rs137854455 rs1554686162 rs397516433
Ask Dr. Hemsworth about this variant