Variants in gene combination CYP21A2, LOC106780800 with conflicting interpretations reported as "likely benign and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (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_000500.9(CYP21A2):c.803C>T (p.Pro268Leu)	rs61732108	0.00090
NM_000500.9(CYP21A2):c.318G>A (p.Pro106=)	rs6455
NM_000500.9(CYP21A2):c.552C>G (p.Asp184Glu)	rs397515531

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