List of variants reported as benign for Intellectual disability, autosomal dominant 20

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Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_002397.5(MEF2C):c.811-13C>T	rs201988423	0.00113
NM_002397.5(MEF2C):c.834+15C>T	rs140447603	0.00097
NM_002397.5(MEF2C):c.811-12G>A	rs149706617	0.00064
NM_002397.5(MEF2C):c.402+16A>G	rs373582392	0.00050
NM_002397.5(MEF2C):c.642C>T (p.Asn214=)	rs79455305	0.00011
NM_002397.5(MEF2C):c.1207A>G (p.Thr403Ala)	rs753002290	0.00010
NM_002397.5(MEF2C):c.180C>T (p.Thr60=)	rs773278207	0.00010
NM_002397.5(MEF2C):c.363C>T (p.Asn121=)	rs186648089	0.00008
NM_002397.5(MEF2C):c.258+10C>T	rs563149132	0.00004
NM_002397.5(MEF2C):c.1021G>A (p.Ala341Thr)	rs797045703	0.00001
NM_002397.5(MEF2C):c.499C>T (p.Pro167Ser)	rs1322552264	0.00001
NM_002397.5(MEF2C):c.730A>G (p.Met244Val)	rs752349182	0.00001
NM_002397.5(MEF2C):c.963C>T (p.Thr321=)	rs1363064582	0.00001
NM_002397.5(MEF2C):c.1029C>G (p.His343Gln)	rs796052727
NM_002397.5(MEF2C):c.1087C>T (p.Leu363Phe)	rs2152207244
NM_002397.5(MEF2C):c.1100+6C>G	rs1759908843
NM_002397.5(MEF2C):c.1331A>C (p.His444Pro)	rs1554098567
NM_002397.5(MEF2C):c.1385T>C (p.Val462Ala)	rs1194300256
NM_002397.5(MEF2C):c.375T>G (p.Asp125Glu)	rs2152673396
NM_002397.5(MEF2C):c.439A>G (p.Ile147Val)
NM_002397.5(MEF2C):c.539A>G (p.Asn180Ser)
NM_002397.5(MEF2C):c.557T>C (p.Val186Ala)	rs1561821810
NM_002397.5(MEF2C):c.589G>C (p.Gly197Arg)	rs1310323196
NM_002397.5(MEF2C):c.638-14dup	rs754587449
NM_002397.5(MEF2C):c.638-9del
NM_002397.5(MEF2C):c.694T>G (p.Leu232Val)	rs2152280607
NM_002397.5(MEF2C):c.965-6_965-2del	rs1064795146

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