RS886041858 MYT1L

Health Risk Chr 2:1912024
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What This Variant Does
"CLNSIG=5
Associated Conditions
Intellectual disability
autosomal dominant 39
Intellectual disability
autosomal dominant 39
Other Variants in MYT1L
rs869320675 rs869320676 rs878853045 rs886041944 rs886041655 rs1057519560 rs1064794713 rs1064793449 rs1064793635 rs1553324416
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