Variants in gene COL6A3 with conflicting interpretations "likely pathogenic" and "likely benign"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_004369.4(COL6A3):c.7258C>T (p.Arg2420Trp)	rs150165484	0.00131
NM_004369.4(COL6A3):c.8189C>A (p.Ala2730Asp)	rs138466455	0.00110
NM_004369.4(COL6A3):c.9128G>A (p.Arg3043His)	rs552651651	0.00025
NM_004369.4(COL6A3):c.6898G>A (p.Gly2300Arg)	rs763348222	0.00006
NM_004369.4(COL6A3):c.4121A>T (p.Asp1374Val)	rs766488017	0.00004
NM_004369.4(COL6A3):c.3844G>A (p.Val1282Met)	rs535661345

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