ClinVar for MedGen (Select 233279) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 559990	NM_000059.4(BRCA2):c.82_147del (p.Leu29_Ser50del)	BRCA2	Deletion (inframe_deletion)	Ovarian serous surface papillary adenocarcinoma	GLikely pathogenic
Select item 37534	NM_007294.4(BRCA1):c.3627dup (p.Glu1210fs)	BRCA1, LOC126862571 (E1163fs +21 more)	Duplication (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic