Variants with conflicting interpretations "uncertain significance" from Molecular Genetics and Enzymology, National Research Centre and "benign" from PreventionGenetics, part of Exact Sciences

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:
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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_001308093.3(GATA4):c.1000+56C>A	rs804280	0.61291
NM_181486.4(TBX5):c.663+36G>T	rs2236017	0.54802

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