Variants with conflicting interpretations "benign" from Center of Medical Genetics and Primary Health Care and "likely benign" from any submitter

Minimum review status of the submission from Center of Medical Genetics and Primary Health Care:		Collection method of the submission from Center of Medical Genetics and Primary Health Care:
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_000059.4(BRCA2):c.9976A>T (p.Lys3326Ter)	rs11571833	0.00597
NM_032043.3(BRIP1):c.790C>T (p.Arg264Trp)	rs28997569	0.00104
NM_000051.4(ATM):c.1744T>C (p.Phe582Leu)	rs2235006	0.00071

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