List of variants in gene combination RAD51D, RAD51L3-RFFL reported as benign for not provided

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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: 27

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HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.480+187T>C	rs936656	0.50511
NM_002878.4(RAD51D):c.234C>T (p.Ser78=)	rs9901455	0.15951
NM_002878.4(RAD51D):c.494G>A (p.Arg165Gln)	rs4796033	0.11973
NM_002878.4(RAD51D):c.481-205A>G	rs8071313	0.10477
NM_002878.4(RAD51D):c.263+1920C>T	rs28363264	0.10429
NM_002878.4(RAD51D):c.739-103T>C	rs28363289	0.07644
NM_002878.4(RAD51D):c.263+1750G>A	rs9915609	0.05506
NC_000017.11:g.35120008C>T	rs114893073	0.03378
NM_002878.4(RAD51D):c.481-144T>C	rs8067218	0.02661
NM_002878.4(RAD51D):c.480+75T>G	rs8067688	0.02645
NM_002878.4(RAD51D):c.738+131G>T	rs28363285	0.02447
NM_002878.4(RAD51D):c.698A>G (p.Glu233Gly)	rs28363284	0.01102
NM_002878.4(RAD51D):c.-38G>T	rs114252524	0.00868
NM_002878.4(RAD51D):c.873C>T (p.Arg291=)	rs140848654	0.00399
NM_002878.4(RAD51D):c.771C>T (p.Ser257=)	rs146212490	0.00206
NM_002878.4(RAD51D):c.481-7G>A	rs145832514	0.00171
NM_002878.4(RAD51D):c.568G>A (p.Ala190Thr)	rs80116829	0.00167
NM_002878.4(RAD51D):c.666A>G (p.Glu222=)	rs114012742	0.00131
NM_002878.4(RAD51D):c.263+1474C>T	rs201720876	0.00016
NM_002878.4(RAD51D):c.346-10C>T	rs779972784	0.00005
NM_002878.4(RAD51D):c.792C>G (p.Leu264=)	rs536544621	0.00002
NM_002878.4(RAD51D):c.739-10T>C	rs199998187	0.00001
NM_002878.4(RAD51D):c.904-13C>A	rs964696175	0.00001
NM_002878.4(RAD51D):c.*130A>C	rs28363292
NM_002878.4(RAD51D):c.263+1571T>C
NM_002878.4(RAD51D):c.263+94dup	rs147268486
NM_002878.4(RAD51D):c.481-80G>T	rs28363273

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