RS191317359 MYT1L

Health Risk Chr 2:1979757
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Associated Conditions
Inborn genetic diseases
Intellectual disability
autosomal dominant 39
MYT1L-related disorder
Inborn genetic diseases
Intellectual disability
autosomal dominant 39
MYT1L-related disorder
Other Variants in MYT1L
rs869320675 rs869320676 rs878853045 rs886041944 rs886041858 rs886041655 rs1057519560 rs1064794713 rs1064793449 rs1064793635
Ask Dr. Hemsworth about this variant