Variants in gene COL18A1 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	gnomAD frequency
NM_001379500.1(COL18A1):c.2338C>T (p.Gln780Ter)	rs786205554	0.00001
NM_001379500.1(COL18A1):c.1593del (p.Pro534fs)	rs778909108

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