List of variants reported as uncertain significance for Malignant tumor of pancreas

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.440A>G (p.Gln147Arg)	rs80358674	0.00025
NM_000059.4(BRCA2):c.6325G>A (p.Val2109Ile)	rs79456940	0.00006
NM_000059.4(BRCA2):c.7522G>A (p.Gly2508Ser)	rs80358978	0.00004
NM_000059.4(BRCA2):c.2671G>C (p.Val891Leu)	rs756951335	0.00002
NM_000059.4(BRCA2):c.353G>A (p.Arg118His)	rs80358603	0.00002
NM_000059.4(BRCA2):c.10150C>T (p.Arg3384Ter)	rs397507568	0.00001
NM_000059.4(BRCA2):c.10131A>C (p.Glu3377Asp)	rs1064793835
NM_000059.4(BRCA2):c.9206G>A (p.Cys3069Tyr)	rs587782091
NM_000059.4(BRCA2):c.92G>T (p.Trp31Leu)	rs397508045
NM_007294.4(BRCA1):c.1769_1771del (p.Ser590del)	rs1555591267
NM_007294.4(BRCA1):c.3327_3329del (p.Lys1110del)	rs80357575
NM_007294.4(BRCA1):c.4271A>G (p.Gln1424Arg)	rs1555584133
NM_007294.4(BRCA1):c.4456A>T (p.Ser1486Cys)	rs397507232

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