Variants with conflicting interpretations "pathogenic" from Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital and "likely pathogenic" from Invitae

Minimum review status of the submission from Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital:		Collection method of the submission from Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital:
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_000891.3(KCNJ2):c.913A>G (p.Thr305Ala)	rs199473387
NM_001042492.3(NF1):c.6001G>A (p.Gly2001Arg)	rs199474751
NM_004006.3(DMD):c.10098AGA[1] (p.Glu3367del)	rs886042840

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