List of variants in gene combination RAD51D, RAD51L3-RFFL reported as likely pathogenic by Counsyl

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.363del (p.Ala122fs)	rs730881935	0.00002
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.1A>G (p.Met1Val)	rs561425038
NM_002878.4(RAD51D):c.1A>T (p.Met1Leu)	rs561425038
NM_002878.4(RAD51D):c.270_271dup (p.Lys91fs)	rs753862052
NM_002878.4(RAD51D):c.6_13dup (p.Arg5fs)	rs1555570506
NM_002878.4(RAD51D):c.740_741dup (p.Thr248Ter)	rs1555567197
NM_002878.4(RAD51D):c.81del (p.Val28fs)	rs1064793952
NM_002878.4(RAD51D):c.85del (p.Val29fs)	rs1057517586
NM_002878.4(RAD51D):c.94_95del (p.Val32fs)	rs786203137

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