Variants with conflicting interpretations "benign" from GeneDx and "likely benign" 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000352.6(ABCC8):c.1158C>T (p.Asn386=)	rs60824529	0.01375
NM_005629.4(SLC6A8):c.1768-3C>T	rs150207268	0.00435
NM_004006.3(DMD):c.1184G>A (p.Arg395Gln)	rs148511512	0.00006

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