List of variants reported as likely benign for Meckel syndrome, type 4

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_025114.4(CEP290):c.4119A>G (p.Lys1373=)	rs117122459	0.02390
NM_025114.4(CEP290):c.251-10A>T	rs190383141	0.02052
NM_025114.4(CEP290):c.829G>C (p.Glu277Gln)	rs45502896	0.01608
NM_025114.4(CEP290):c.3465G>A (p.Leu1155=)	rs150138016	0.00815
NM_025114.4(CEP290):c.5199A>G (p.Gln1733=)	rs79644671	0.00740
NM_025114.4(CEP290):c.1624-5T>C	rs142742071	0.00704
NM_025114.4(CEP290):c.2827A>G (p.Ile943Val)	rs75220808	0.00678
NM_025114.4(CEP290):c.5237G>A (p.Arg1746Gln)	rs61941020	0.00577
NM_025114.4(CEP290):c.1079G>A (p.Arg360Gln)	rs188164241	0.00405
NM_025114.4(CEP290):c.1298A>G (p.Asp433Gly)	rs200211587	0.00146

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