RS1060503383 SYNGAP1

Health Risk Chr 6:33441318
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What This Variant Does
"CLNSIG=5
Associated Conditions
Intellectual disability
autosomal dominant 5
13 conditions
See cases
Inborn genetic diseases
Intellectual disability
autosomal dominant 5
13 conditions
See cases
Inborn genetic diseases
Other Variants in SYNGAP1
rs121918315 rs121918316 rs397515320 rs2151161019 rs1581995953 rs1554121970 rs1581987445 rs397514670 rs397514741 rs587780470
Ask Dr. Hemsworth about this variant