List of variants in gene combination RAD51D, RAD51L3-RFFL reported as pathogenic for breast carcinoma

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.480+1G>A	rs1597862471
NM_002878.4(RAD51D):c.757C>T (p.Arg253Ter)	rs137886232
NM_002878.4(RAD51D):c.790_796dup (p.Arg266fs)	rs2142411968

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