List of variants in gene combination RAD51D, RAD51L3-RFFL reported as pathogenic by Hereditary Cancer Group, L’Institut d'Investigació Biomèdica de Bellvitge

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.144+1G>T	rs2142477107
NM_002878.4(RAD51D):c.146_263+1del	rs2142473486
NM_002878.4(RAD51D):c.215del (p.Tyr72fs)	rs2142474090
NM_002878.4(RAD51D):c.24_27del (p.Cys9fs)	rs2142480769
NM_002878.4(RAD51D):c.264-1G>A	rs2091622013
NM_002878.4(RAD51D):c.754del (p.Thr252fs)	rs2142412448

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