List of variants reported as benign for breast disorder by Leiden Open Variation Database

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_024675.4(PALB2):c.2586+58C>T	rs249954	0.31139
NM_024675.4(PALB2):c.1684+1597T>C	rs16940342	0.18113
NM_024675.4(PALB2):c.2997-624G>C	rs447529	0.12992
NM_024675.4(PALB2):c.3113+1376C>G	rs369444	0.07316
NM_024675.4(PALB2):c.-47G>A	rs8053188	0.04991
NM_024675.4(PALB2):c.212-58A>C	rs80291632	0.02171
NM_024675.4(PALB2):c.629C>T (p.Pro210Leu)	rs57605939	0.02101
NM_024675.4(PALB2):c.1684+29A>G	rs74320059	0.01884
NM_024675.4(PALB2):c.1419A>C (p.Pro473=)	rs62625275	0.00309
NM_024675.4(PALB2):c.1470C>T (p.Pro490=)	rs45612837	0.00035
NM_024675.4(PALB2):c.212-33A>C	rs515726079	0.00003
NM_024675.4(PALB2):c.1038A>G (p.Lys346=)	rs515726059	0.00001
NM_024675.4(PALB2):c.1380A>G (p.Gln460=)	rs372641262	0.00001
NM_024675.4(PALB2):c.1317G>A (p.Gly439=)	rs515726066
NM_024675.4(PALB2):c.1461C>T (p.Val487=)	rs515726069
NM_024675.4(PALB2):c.999C>T (p.Thr333=)	rs180177096
NM_032486.4(DCTN5):c.-27C>G	rs515726057

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