Variants in gene CTRC with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 10

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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.640-12G>A	rs183053579	0.00194
NM_007272.3(CTRC):c.494-6C>T	rs111790169	0.00096
NM_007272.3(CTRC):c.640-14C>T	rs202049497	0.00060
NM_007272.3(CTRC):c.703G>A (p.Val235Ile)	rs140993290	0.00024
NM_007272.3(CTRC):c.674A>C (p.Glu225Ala)	rs201486613	0.00020
NM_007272.3(CTRC):c.533A>G (p.Gln178Arg)	rs200678111	0.00009
NM_007272.3(CTRC):c.369C>T (p.Ala123=)	rs749606141	0.00001
NM_007272.3(CTRC):c.68C>T (p.Pro23Leu)	rs533967597	0.00001
NM_007272.3(CTRC):c.-59C>T	rs183658182

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