RS587783747 MEF2C

Health Risk Chr 5:88751881
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Neurodevelopmental disorder with hypotonia
stereotypic hand movements
and impaired language
Inborn genetic diseases
MEF2C-related disorder
Neurodevelopmental disorder with hypotonia
stereotypic hand movements
and impaired language
Inborn genetic diseases
MEF2C-related disorder
Other Variants in MEF2C
rs267607233 rs397514655 rs2153074822 rs397514656 rs730882192 rs398123686 rs587783749 rs786200981 rs781632867 rs368575766
Ask Dr. Hemsworth about this variant