List of variants reported as pathogenic for Leber congenital amaurosis 15 by OMIM

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_003322.6(TULP1):c.1102G>T (p.Gly368Trp)	rs387906837
NM_003322.6(TULP1):c.1198C>T (p.Arg400Trp)	rs387906836
NM_003322.6(TULP1):c.1204G>T (p.Glu402Ter)	rs387906835
NM_003322.6(TULP1):c.1582_1587dup (p.Ala529_Ile530insPheAla)	rs2150921548
NM_003322.6(TULP1):c.99+1G>A	rs281865166

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