List of variants reported as uncertain significance for age-related macular degeneration by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000350.3(ABCA4):c.5603A>T (p.Asn1868Ile)	rs1801466	0.04126
NM_000350.3(ABCA4):c.5843C>T (p.Pro1948Leu)	rs56142141	0.03191
NM_000350.3(ABCA4):c.4253+43G>A	rs61754045	0.00486
NM_000350.3(ABCA4):c.2588G>C (p.Gly863Ala)	rs76157638	0.00445
NM_000350.3(ABCA4):c.5693G>A (p.Arg1898His)	rs1800552	0.00153
NM_000350.3(ABCA4):c.2690C>T (p.Thr897Ile)	rs61749440	0.00133
NM_000350.3(ABCA4):c.514G>A (p.Gly172Ser)	rs61748532	0.00033
NM_000350.3(ABCA4):c.3608G>A (p.Gly1203Glu)	rs146786552	0.00019
NM_000350.3(ABCA4):c.4909G>A (p.Ala1637Thr)	rs61754056	0.00008
NM_001319074.4(RAX2):c.236G>A (p.Arg79Gln)	rs779301810	0.00005
NM_000350.3(ABCA4):c.3670T>G (p.Cys1224Gly)	rs762213896	0.00003
NM_000350.3(ABCA4):c.5645T>C (p.Met1882Thr)	rs780817685	0.00001
NM_000350.3(ABCA4):c.2318A>G (p.Tyr773Cys)	rs764727316
NM_000350.3(ABCA4):c.6453G>T (p.Met2151Ile)	rs1057518954
NM_000350.3(ABCA4):c.676C>A (p.Arg226Ser)	rs149780335
NM_000350.3(ABCA4):c.785A>G (p.Asp262Gly)	rs1661753710

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