List of variants reported as likely benign for Intellectual disability, autosomal dominant 45

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001386298.1(CIC):c.7510T>C (p.Ser2504Pro)	rs745695673	0.00775
NM_001386298.1(CIC):c.3933A>G (p.Ala1311=)	rs112950169	0.00325
NM_001386298.1(CIC):c.577A>T (p.Thr193Ser)	rs547565552	0.00316
NM_001386298.1(CIC):c.6611C>T (p.Pro2204Leu)	rs374363627	0.00025
NM_001386298.1(CIC):c.6313G>A (p.Ala2105Thr)	rs199898619	0.00008
NM_001386298.1(CIC):c.4928C>T (p.Ser1643Leu)	rs587778197	0.00003
NM_001386298.1(CIC):c.2468A>G (p.Lys823Arg)	rs775387226	0.00002
NM_001386298.1(CIC):c.3180-10C>G	rs28469564
NM_001386298.1(CIC):c.4462G>A (p.Gly1488Arg)	rs2038007181
NM_001386298.1(CIC):c.6173C>G (p.Thr2058Ser)	rs2038239333

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