Variants with conflicting interpretations "likely pathogenic" from GeneDx and "drug response" 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_005228.5(EGFR):c.2369C>T (p.Thr790Met)	rs121434569	0.00006
NM_000492.4(CFTR):c.3208C>T (p.Arg1070Trp)	rs202179988	0.00003
NM_000540.3(RYR1):c.6488G>A (p.Arg2163His)	rs118192163
NM_000540.3(RYR1):c.9310G>A (p.Glu3104Lys)	rs193922832
NM_000540.3(RYR1):c.982C>T (p.Arg328Trp)	rs193922762

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