Variants with conflicting interpretations "likely pathogenic" from Cancer Genomics Group, Japanese Foundation For Cancer Research and "pathogenic" 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.5576_5579del (p.Ile1859fs)	rs80359520
NM_000059.4(BRCA2):c.658_659del (p.Val220fs)	rs80359604
NM_000059.4(BRCA2):c.6649A>T (p.Lys2217Ter)	rs1555284779
NM_002878.4(RAD51D):c.270_271dup (p.Lys91fs)	rs753862052
NM_007294.4(BRCA1):c.2764_2767del (p.Thr922fs)	rs80357822
Single allele

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