List of variants reported as likely pathogenic for Fanconi anemia complementation group N; Pancreatic cancer, susceptibility to, 3; Breast-ovarian cancer, familial, susceptibility to, 5 by Fulgent Genetics, Fulgent Genetics

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_024675.4(PALB2):c.3113+5G>C	rs876659463	0.00001
NM_024675.4(PALB2):c.109-2A>G	rs730881897
NM_024675.4(PALB2):c.1183del (p.Ser395fs)	rs1555461415
NM_024675.4(PALB2):c.2748+1G>A	rs753153576
NM_024675.4(PALB2):c.3087del (p.Thr1030fs)
NM_024675.4(PALB2):c.3351-1G>A	rs1597062406
NM_024675.4(PALB2):c.3441T>A (p.Cys1147Ter)	rs1555457867
NM_024675.4(PALB2):c.71_73delinsGG (p.Leu24fs)	rs1967112121
NM_024675.4(PALB2):c.892_893del (p.Val298fs)	rs2142431841
NM_024675.4:c.3179_3180insALU

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