List of variants reported as likely benign for Leber congenital amaurosis 6

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Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_020366.4(RPGRIP1):c.3340-15C>T	rs28664100	0.05325
NM_020366.4(RPGRIP1):c.3341A>G (p.Asp1114Gly)	rs17103671	0.02649
NM_020366.4(RPGRIP1):c.3719G>A (p.Gly1240Glu)	rs34725281	0.02464
NM_020366.4(RPGRIP1):c.*10T>C	rs80191010	0.01626
NM_020366.4(RPGRIP1):c.3546C>T (p.Asp1182=)	rs34116882	0.01609
NM_020366.4(RPGRIP1):c.2878G>C (p.Ala960Pro)	rs35810926	0.00369
NM_020366.4(RPGRIP1):c.1767G>T (p.Gln589His)	rs34067949	0.00344
NM_020366.4(RPGRIP1):c.218+13C>G	rs200225522	0.00279
NM_020366.4(RPGRIP1):c.2284C>T (p.Leu762=)	rs145896974	0.00240
NM_020366.4(RPGRIP1):c.2376G>A (p.Ser792=)	rs185667326	0.00183
NM_020366.4(RPGRIP1):c.1753C>T (p.Pro585Ser)	rs147586703	0.00155
NM_020366.4(RPGRIP1):c.95T>A (p.Met32Lys)	rs200510462	0.00140
NM_020366.4(RPGRIP1):c.450C>G (p.Leu150=)	rs144585562	0.00130
NM_020366.4(RPGRIP1):c.542C>G (p.Ala181Gly)	rs186266220	0.00127
NM_020366.4(RPGRIP1):c.2555G>A (p.Arg852Gln)	rs181758389	0.00076
NM_020366.4(RPGRIP1):c.74C>T (p.Pro25Leu)	rs199590641	0.00073
NM_020366.4(RPGRIP1):c.3171C>T (p.His1057=)	rs201838837	0.00053
NM_020366.4(RPGRIP1):c.2550G>A (p.Gln850=)	rs200268506	0.00051
NM_020366.4(RPGRIP1):c.1078-9C>A	rs371312060	0.00042
NM_020366.4(RPGRIP1):c.1920C>T (p.Ala640=)	rs368434311	0.00029
NM_020366.4(RPGRIP1):c.2435G>A (p.Arg812Gln)	rs190490019	0.00024
NM_020366.4(RPGRIP1):c.1236G>A (p.Gln412=)	rs140904308	0.00014
NM_020366.4(RPGRIP1):c.658A>G (p.Met220Val)	rs371762530	0.00011
NM_020366.4(RPGRIP1):c.2334T>C (p.Asp778=)	rs188318743	0.00010
NM_020366.4(RPGRIP1):c.1401A>G (p.Gln467=)	rs184853466	0.00002
NM_020366.4(RPGRIP1):c.3239-14C>T	rs542859849	0.00001
NM_020366.4(RPGRIP1):c.3448G>T (p.Asp1150Tyr)	rs144704092
NM_020366.4(RPGRIP1):c.3571C>T (p.Arg1191Trp)	rs188660364

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