List of variants in gene combination RAD51D, RAD51L3-RFFL reported as likely pathogenic for Breast and/or ovarian cancer

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.620C>T (p.Ser207Leu)	rs370228071	0.00003
NM_002878.4(RAD51D):c.898C>T (p.Arg300Ter)	rs750621215	0.00002
NM_002878.4(RAD51D):c.345+2T>C	rs876659394
NM_002878.4(RAD51D):c.748del (p.His250fs)	rs587780105

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