List of variants reported as uncertain significance for adenocarcinoma by 3DMed Clinical Laboratory Inc

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_004360.5(CDH1):c.1018A>G (p.Thr340Ala)	rs116093741	0.00022
NM_000038.6(APC):c.2527A>G (p.Ser843Gly)	rs536223189	0.00006
NM_000038.6(APC):c.8332G>T (p.Ala2778Ser)	rs587778046	0.00006
NM_000038.6(APC):c.1984C>A (p.Leu662Ile)	rs756859993	0.00002
NM_005228.5(EGFR):c.2270A>G (p.Lys757Arg)	rs397517102	0.00002
NM_000038.6(APC):c.811A>G (p.Met271Val)	rs587781464	0.00001
NM_000059.4(BRCA2):c.4376A>G (p.Asn1459Ser)	rs117187202	0.00001
NM_000038.6(APC):c.1463T>C (p.Leu488Pro)	rs368434773
NM_000038.6(APC):c.2558A>G (p.Glu853Gly)	rs1554084263
NM_000038.6(APC):c.3160C>T (p.His1054Tyr)	rs1195583636
NM_000038.6(APC):c.4440G>C (p.Gln1480His)	rs876659881
NM_000038.6(APC):c.4658C>T (p.Ala1553Val)	rs1554086050
NM_000038.6(APC):c.6152A>G (p.Lys2051Arg)	rs1554087256
NM_000038.6(APC):c.7832C>T (p.Thr2611Ile)	rs587778037
NM_000038.6(APC):c.8461G>A (p.Asp2821Asn)	rs1554089164

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