Variants with conflicting interpretations "pathogenic" from Counsyl and "likely benign" from any submitter

Minimum review status of the submission from Counsyl:		Collection method of the submission from Counsyl:
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_004004.6(GJB2):c.71G>A (p.Trp24Ter)	rs104894396	0.00002
NM_000546.6(TP53):c.844C>T (p.Arg282Trp)	rs28934574	0.00001

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