List of variants reported as uncertain significance for cataract 4 multiple types

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_006891.4(CRYGD):c.168C>G (p.Tyr56Ter)	rs202233735	0.00627
NM_006891.4(CRYGD):c.482A>G (p.Asn161Ser)	rs760434926	0.00005
NM_006891.4(CRYGD):c.-33A>G	rs1044458149	0.00003
NM_006891.4(CRYGD):c.295A>G (p.Arg99Gly)	rs886055527	0.00001
NM_006891.4(CRYGD):c.233C>T (p.Ser78Phe)	rs2105853718
NM_006891.4(CRYGD):c.252C>T (p.His84=)	rs775032143
NM_006891.4(CRYGD):c.290A>T (p.Asp97Val)
NM_006891.4(CRYGD):c.333T>C (p.Cys111=)	rs933732267

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