List of variants reported as uncertain significance for Intellectual disability, autosomal dominant 5 by New York Genome Center

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_006772.3(SYNGAP1):c.1904A>G (p.Asn635Ser)	rs775566992	0.00006
NM_006772.3(SYNGAP1):c.1118G>T (p.Gly373Val)	rs774819723	0.00002
NM_006772.3(SYNGAP1):c.1285C>T (p.Arg429Trp)	rs748333558	0.00002
NM_006772.3(SYNGAP1):c.1286G>A (p.Arg429Gln)	rs772336493	0.00002
NM_006772.3(SYNGAP1):c.514C>T (p.Arg172Trp)	rs142649710	0.00001
NM_006772.3(SYNGAP1):c.1586T>C (p.Ile529Thr)	rs2151172455
NM_006772.3(SYNGAP1):c.1913+5G>A	rs1761021575
NM_006772.3(SYNGAP1):c.2596G>A (p.Val866Ile)	rs768878991
NM_006772.3(SYNGAP1):c.2854G>A (p.Gly952Ser)	rs1038956173
NM_006772.3(SYNGAP1):c.295+1551G>A	rs2151138610
NM_006772.3(SYNGAP1):c.3394T>C (p.Ser1132Pro)	rs2151191235
NM_006772.3(SYNGAP1):c.3835G>A (p.Ala1279Thr)	rs1165427519

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