Variants in gene RPE65 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 3

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HGVS	dbSNP	gnomAD frequency
NM_000329.3(RPE65):c.859-11C>T	rs369772824	0.00010
NM_000329.3(RPE65):c.1129-5C>T	rs368533067	0.00004
NM_000329.3(RPE65):c.353+7G>A	rs773557127	0.00002

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