List of variants in gene combination ABCA4, LOC126805793 reported as likely benign for retinal disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000350.3(ABCA4):c.4925G>T (p.Ser1642Ile)	rs114518437	0.00425
NM_000350.3(ABCA4):c.4771G>A (p.Gly1591Arg)	rs113106943	0.00239

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