RS201961477 MYT1L

Health Risk Chr 2:1889300
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Associated Conditions
Intellectual disability
autosomal dominant 39
Inborn genetic diseases
Intellectual disability
autosomal dominant 39
Inborn genetic diseases
Other Variants in MYT1L
rs869320675 rs869320676 rs878853045 rs886041944 rs886041858 rs886041655 rs1057519560 rs1064794713 rs1064793449 rs1064793635
Ask Dr. Hemsworth about this variant