RS1131691979 SYNGAP1

Health Risk Chr 6:33432198
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Associated Conditions
Infantile epilepsy syndrome
Inborn genetic diseases
Intellectual disability
autosomal dominant 5
Infantile epilepsy syndrome
Inborn genetic diseases
Intellectual disability
autosomal dominant 5
Other Variants in SYNGAP1
rs121918315 rs121918316 rs397515320 rs2151161019 rs1581995953 rs1554121970 rs1581987445 rs397514670 rs397514741 rs587780470
Ask Dr. Hemsworth about this variant