ClinVar Miner

List of variants reported as benign for breast-ovarian cancer, familial, susceptibility to, 4 by Invitae

Included ClinVar conditions (1):
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Total variants: 22
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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.698A>G (p.Glu233Gly) rs28363284 0.01102
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.146C>T (p.Ala49Val) rs140317560 0.00116
NM_002878.4(RAD51D):c.932T>A (p.Ile311Asn) rs145309168 0.00041
NM_002878.4(RAD51D):c.904-11T>A rs374449943 0.00038
NM_002878.4(RAD51D):c.216C>T (p.Tyr72=) rs148690585 0.00028
NM_002878.4(RAD51D):c.196G>A (p.Val66Met) rs56026142 0.00009
NM_002878.4(RAD51D):c.145-14G>C rs200470533 0.00004
NM_002878.4(RAD51D):c.83-20T>C rs182793287 0.00002
NM_002878.4(RAD51D):c.346-3del rs2142434112
NM_002878.4(RAD51D):c.481-23_481-20del rs760861758
NM_002878.4(RAD51D):c.668-13CCT[2] rs1230625396
NM_002878.4(RAD51D):c.738+14C>T rs374761868
NM_002878.4(RAD51D):c.904-12TTC[2] rs779850240

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