RS1057518796 SYNGAP1

Health Risk Chr 6:33443751
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Cerebellar ataxia
Global developmental delay
Absent speech
Intellectual disability
autosomal dominant 5
Cerebellar ataxia
Global developmental delay
Absent speech
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