RS587783749 MEF2C

Health Risk Chr 5:88730212
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What This Variant Does
"CLNSIG=5
Associated Conditions
Neurodevelopmental disorder with hypotonia
stereotypic hand movements
and impaired language
Inborn genetic diseases
Neurodevelopmental disorder with hypotonia
stereotypic hand movements
and impaired language
Inborn genetic diseases
Other Variants in MEF2C
rs267607233 rs397514655 rs2153074822 rs397514656 rs730882192 rs398123686 rs587783747 rs786200981 rs781632867 rs368575766
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