Variants with conflicting interpretations "uncertain significance" from Cancer Genomics Group, Japanese Foundation For Cancer Research and "likely benign" from any submitter

Minimum review status of the submission from Cancer Genomics Group, Japanese Foundation For Cancer Research:		Collection method of the submission from Cancer Genomics Group, Japanese Foundation For Cancer Research:
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_007194.4(CHEK2):c.538C>T (p.Arg180Cys)	rs77130927	0.00051
NM_000465.4(BARD1):c.773T>C (p.Ile258Thr)	rs146223579	0.00004

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