C3150659[trait identifier] AND "MGZ Medical Genetics Center"[submitter - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 182841	NM_058216.3(RAD51C):c.29T>G (p.Met10Arg)	RAD51C (M10R)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 241769	NM_058216.3(RAD51C):c.274G>A (p.Glu92Lys)	RAD51C (E92K)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 860928	NM_058216.3(RAD51C):c.379_380insG (p.Pro127fs)	RAD51C (P127fs)	Insertion (frameshift variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic/Likely pathogenic
Select item 140849	NM_058216.3(RAD51C):c.577C>T (p.Arg193Ter)	RAD51C (R193*)	Single nucleotide variant (nonsense +1 more)	RAD51C-related disorder +6 more	GPathogenic/Likely pathogenic
Select item 1709992	NM_058216.3(RAD51C):c.829A>T (p.Arg277Ter)	RAD51C (R277*)	Single nucleotide variant (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3	GPathogenic/Likely pathogenic
Select item 141768	NM_058216.3(RAD51C):c.905-2_905-1del	RAD51C	Deletion (splice acceptor variant)	Hereditary cancer-predisposing syndrome +5 more	GPathogenic/Likely pathogenic

ClinVar