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

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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: 25

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HGVS	dbSNP	gnomAD frequency
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.903+53C>T	rs45496096	0.01225
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.695G>A (p.Arg232Gln)	rs28363283	0.00457
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+1588A>G	rs180869630	0.00123
NM_002878.4(RAD51D):c.919G>A (p.Glu307Lys)	rs115031549	0.00083
NM_002878.4(RAD51D):c.263+1570T>A	rs376472075	0.00078
NM_002878.4(RAD51D):c.216C>T (p.Tyr72=)	rs148690585	0.00028
NM_002878.4(RAD51D):c.263+1605G>A	rs147933658	0.00023
NM_002878.4(RAD51D):c.983C>T (p.Thr328Ile)	rs138969595	0.00021
NM_002878.4(RAD51D):c.*7C>T	rs370985675	0.00019
NM_002878.4(RAD51D):c.904-3C>T	rs45478491	0.00018
NM_002878.4(RAD51D):c.145-40C>T	rs370850037	0.00011
NM_002878.4(RAD51D):c.196G>A (p.Val66Met)	rs56026142	0.00009
NM_002878.4(RAD51D):c.864C>T (p.Gly288=)	rs138557828	0.00009
NM_002878.4(RAD51D):c.576+18C>T	rs752051995	0.00001
NM_002878.4(RAD51D):c.145-39G>T	rs7207508
NM_002878.4(RAD51D):c.904-12TTC[2]	rs779850240

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