Variants with conflicting interpretations "pathogenic" from Department of Genetics, Robert DEBRE University Hospital and "likely pathogenic" from any submitter

Minimum review status of the submission from Department of Genetics, Robert DEBRE University Hospital:		Collection method of the submission from Department of Genetics, Robert DEBRE University 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001101.5(ACTB):c.193C>T (p.Leu65Phe)	rs281875332
NM_001101.5(ACTB):c.220G>A (p.Gly74Ser)	rs587779770
NM_001101.5(ACTB):c.625G>A (p.Val209Met)	rs587779777
NM_001958.5(EEF1A2):c.1295C>T (p.Thr432Met)	rs2082362479
NM_001958.5(EEF1A2):c.1309G>T (p.Val437Phe)	rs1057521655
NM_001958.5(EEF1A2):c.271G>A (p.Asp91Asn)	rs886041197
NM_001958.5(EEF1A2):c.370G>A (p.Glu124Lys)	rs886042041
NM_001958.5(EEF1A2):c.71C>T (p.Thr24Met)	rs1064795618

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