List of variants reported as uncertain significance for Intellectual disability, autosomal dominant 5 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_006772.3(SYNGAP1):c.4021G>A (p.Ala1341Thr)	rs771224281	0.00006
NM_006772.3(SYNGAP1):c.1851G>T (p.Glu617Asp)
NM_006772.3(SYNGAP1):c.2186A>G (p.Asn729Ser)
NM_006772.3(SYNGAP1):c.3192G>C (p.Gln1064His)
NM_006772.3(SYNGAP1):c.670A>G (p.Thr224Ala)	rs1777305165

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