Variants with conflicting interpretations "uncertain significance" from Laboratory of Molecular Genetics, CHU Rennes and "likely pathogenic" from any submitter

Minimum review status of the submission from Laboratory of Molecular Genetics, CHU Rennes:		Collection method of the submission from Laboratory of Molecular Genetics, CHU Rennes:
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_003709.4(KLF7):c.790G>A (p.Asp264Asn)	rs1057518995

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