Variants with conflicting interpretations "likely pathogenic" from Division of Medical Genetics at University of Versailles, Paris Saclay University and "pathogenic" from any submitter

Minimum review status of the submission from Division of Medical Genetics at University of Versailles, Paris Saclay University:		Collection method of the submission from Division of Medical Genetics at University of Versailles, Paris Saclay University:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 1

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HGVS	dbSNP	gnomAD frequency
NM_000090.4(COL3A1):c.1351G>A (p.Glu451Lys)	rs1559056438

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