Variants in gene RP1 with conflicting interpretations "uncertain significance" and "likely pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) 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_006269.2(RP1):c.121T>C (p.Tyr41His)	rs746359399	0.00004
NM_006269.2(RP1):c.539T>G (p.Phe180Cys)	rs557432569	0.00001
NM_006269.2(RP1):c.3319C>G (p.Gln1107Glu)	rs939932729

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