Variants with conflicting interpretations "pathogenic" from GeneDx and "likely pathogenic" from Natera, Inc.

Minimum review status of the submission from GeneDx:		Collection method of the submission from GeneDx:
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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000492.4(CFTR):c.1766G>A (p.Ser589Asn)	rs397508300	0.00002
NM_000128.4(F11):c.166T>C (p.Cys56Arg)	rs121965069	0.00001
NM_004453.4(ETFDH):c.79C>T (p.Pro27Ser)	rs537038850	0.00001
NM_000094.4(COL7A1):c.3551-3T>G	rs773263825
NM_000492.4(CFTR):c.1219G>T (p.Glu407Ter)	rs766063304

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