Variants in gene CTRC with conflicting interpretations "uncertain significance" and "likely pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 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.217G>A (p.Ala73Thr)	rs515726209	0.00067
NM_007272.3(CTRC):c.181G>A (p.Gly61Arg)	rs769482036	0.00003
NM_007272.3(CTRC):c.649G>A (p.Gly217Ser)	rs202058123	0.00003
NM_007272.3(CTRC):c.494-1G>C	rs766917452	0.00001
NM_007272.3(CTRC):c.132G>A (p.Gln44=)
NM_007272.3(CTRC):c.231-2A>G	rs1570783505
NM_007272.3(CTRC):c.494-1G>A
NM_007272.3(CTRC):c.649G>C (p.Gly217Arg)	rs202058123

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