List of variants reported as benign for Leber congenital amaurosis 1 by Mendelics

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_003322.6(TULP1):c.783G>C (p.Lys261Asn)	rs2064318	0.84569
NM_001122769.3(LCA5):c.71T>C (p.Leu24Ser)	rs2655655	0.84544
NM_003322.6(TULP1):c.776T>C (p.Ile259Thr)	rs2064317	0.36637
NM_001122769.3(LCA5):c.1967G>A (p.Gly656Asp)	rs1875845	0.36167
NM_020366.4(RPGRIP1):c.1639G>T (p.Ala547Ser)	rs10151259	0.21790
NM_014336.5(AIPL1):c.268G>C (p.Asp90His)	rs12449580	0.19586
NM_020366.4(RPGRIP1):c.1793G>A (p.Arg598Gln)	rs74034910	0.01504
NM_020366.4(RPGRIP1):c.2417C>T (p.Thr806Ile)	rs142796310	0.01022

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