Variants with conflicting interpretations "likely pathogenic" from Molecular Genetics and Enzymology, National Research Centre and "benign" from any submitter

Minimum review status of the submission from Molecular Genetics and Enzymology, National Research Centre:		Collection method of the submission from Molecular Genetics and Enzymology, National Research Centre:
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_001308093.3(GATA4):c.1132A>G (p.Ser378Gly)	rs3729856	0.09064

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