Variants with conflicting interpretations "risk factor" from GeneDx and "pathogenic" from any submitter

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_003661.4(APOL1):c.1024A>G (p.Ser342Gly)	rs73885319	0.06773
NM_000038.6(APC):c.3920T>A (p.Ile1307Lys)	rs1801155	0.00116

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