List of variants in gene combination RAD51D, RAD51L3-RFFL reported as pathogenic by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.694C>T (p.Arg232Ter)	rs587780104	0.00004
NM_002878.4(RAD51D):c.556C>T (p.Arg186Ter)	rs387906843	0.00003
NM_002878.4(RAD51D):c.451C>T (p.Gln151Ter)	rs587781756	0.00002
NM_002878.4(RAD51D):c.620C>T (p.Ser207Leu)	rs370228071	0.00002
NM_002878.4(RAD51D):c.649G>T (p.Gly217Ter)	rs775365939	0.00001
NM_002878.4(RAD51D):c.655C>T (p.Gln219Ter)	rs771007945	0.00001
NM_002878.4(RAD51D):c.803G>A (p.Trp268Ter)	rs750219200	0.00001
NM_002878.4(RAD51D):c.270_271dup (p.Lys91fs)	rs753862052
NM_002878.4(RAD51D):c.330dup (p.Ser111Ter)	rs786202434
NM_002878.4(RAD51D):c.649_655delinsTGAGGTT (p.Gly217_Gln219delinsTer)	rs587781527
NM_002878.4(RAD51D):c.748del (p.His250fs)	rs587780105
NM_002878.4(RAD51D):c.904-2A>T	rs1403784434

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