CN239207[trait identifier] AND "Illumina Laboratory Services, Illumina - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 322611	NM_002878.4(RAD51D):c.*871CAGA[1]	RAD51D, RAD51L3-RFFL	Microsatellite (3 prime UTR variant +1 more)	Breast and Ovarian Cancer Susceptibility	GUncertain significance
Select item 322615	NM_002878.4(RAD51D):c.*431CT[1]	RAD51D, RAD51L3-RFFL	Microsatellite (3 prime UTR variant +1 more)	Breast and Ovarian Cancer Susceptibility	GUncertain significance
Select item 322627	NM_002878.4(RAD51D):c.-139C>T	LOC130060715, RAD51D +1 more	Single nucleotide variant (5 prime UTR variant +1 more)	Breast and Ovarian Cancer Susceptibility	GUncertain significance
Select item 324173	NM_058216.3(RAD51C):c.-26C>T	RAD51C	Single nucleotide variant (5 prime UTR variant +1 more)	Breast and Ovarian Cancer Susceptibility +3 more	GBenign/Likely benign
Select item 136157	NM_058216.3(RAD51C):c.195A>G (p.Arg65=)	RAD51C	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +7 more	GBenign/Likely benign
Select item 132702	NM_058216.3(RAD51C):c.859A>G (p.Thr287Ala)	RAD51C (T287A)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +8 more	GBenign/Likely benign
Select item 324174	NM_058216.3(RAD51C):c.*25C>G	RAD51C	Single nucleotide variant (3 prime UTR variant +1 more)	Breast and Ovarian Cancer Susceptibility +3 more	GBenign/Likely benign

ClinVar