Variants with conflicting interpretations "likely pathogenic" from HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology and "pathogenic" from Department of Medical Genetics, Oslo University Hospital

Minimum review status of the submission from HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology:		Collection method of the submission from HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology:
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Show significances as they were submitted (without aggregation into standard terms)

Total variants with conflicting interpretations: 1

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.7024C>T (p.Gln2342Ter)	rs80358928

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