RS1057521747 SCN2A

Health Risk Chr 2:165386976
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Complex neurodevelopmental disorder
Inborn genetic diseases
Complex neurodevelopmental disorder
Other Variants in SCN2A
rs121917749 rs121917750 rs121917751 rs121917752 rs121917753 rs387906683 rs387906684 rs387906685 rs387906686 rs387906687
Ask Dr. Hemsworth about this variant