Variants in gene CTRC with conflicting interpretations "benign" and "pathogenic"

Submission 1 (benign) minimum review status:		Submission 1 (benign) 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	gnomAD frequency
NM_007272.3(CTRC):c.760C>T (p.Arg254Trp)	rs121909293	0.00386
NM_007272.3(CTRC):c.703G>A (p.Val235Ile)	rs140993290	0.00024

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