List of variants in gene combination RAD51D, RAD51L3-RFFL reported as likely benign for Malignant tumor of breast

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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: 11

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HGVS	dbSNP	gnomAD frequency
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.481-7G>A	rs145832514	0.00171
NM_002878.4(RAD51D):c.568G>A (p.Ala190Thr)	rs80116829	0.00167
NM_002878.4(RAD51D):c.919G>A (p.Glu307Lys)	rs115031549	0.00083
NM_002878.4(RAD51D):c.216C>T (p.Tyr72=)	rs148690585	0.00028
NM_002878.4(RAD51D):c.904-3C>T	rs45478491	0.00018
NM_002878.4(RAD51D):c.957G>A (p.Gln319=)	rs147669627	0.00006
NM_002878.4(RAD51D):c.171G>A (p.Leu57=)	rs786202885	0.00002
NM_002878.4(RAD51D):c.27C>T (p.Cys9=)	rs200487648	0.00001
NM_002878.4(RAD51D):c.739-10T>C	rs199998187	0.00001

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