Variants in gene CASR with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (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
NM_000388.4(CASR):c.679C>T (p.Arg227Ter)	rs1085307984
NM_000388.4(CASR):c.73C>T (p.Arg25Ter)	rs201633414

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