Variants in gene PRPH2 with conflicting interpretations "benign" and "likely pathogenic"

Submission 1 (benign) minimum review status:		Submission 1 (benign) 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000322.5(PRPH2):c.37C>T (p.Arg13Trp)	rs61754402	0.00018
NM_000322.5(PRPH2):c.454A>G (p.Met152Val)	rs146703538	0.00002

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