RS1064795331 SYNGAP1

Health Risk Chr 6:33440769
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What This Variant Does
"CLNSIG=4
Associated Conditions
Intellectual disability
autosomal dominant 5
Intellectual disability
autosomal dominant 5
Other Variants in SYNGAP1
rs121918315 rs121918316 rs397515320 rs2151161019 rs1581995953 rs1554121970 rs1581987445 rs397514670 rs397514741 rs587780470
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