List of variants reported as likely benign for Desmoid disease, hereditary; Familial adenomatous polyposis 1; Hepatocellular carcinoma; Gastric cancer; Colorectal cancer; Gastric adenocarcinoma and proximal polyposis of the stomach by Fulgent Genetics, Fulgent Genetics

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.6821C>T (p.Ala2274Val)	rs34919187	0.00088
NM_000038.6(APC):c.4336G>A (p.Ala1446Thr)	rs146572883	0.00056
NM_000038.6(APC):c.2476T>G (p.Leu826Val)	rs145245264	0.00054
NM_000038.6(APC):c.3511C>T (p.Arg1171Cys)	rs201830995	0.00028
NM_000038.6(APC):c.573T>C (p.Tyr191=)	rs185154886	0.00008
NM_000038.6(APC):c.1242C>T (p.Arg414=)	rs751423790	0.00004
NM_000038.6(APC):c.422+10C>G	rs899376835
NM_000038.6(APC):c.423-4del	rs730881230
NM_000038.6(APC):c.423-4dup	rs730881230
NM_000038.6(APC):c.5265_5268delinsATCG (p.Ala1755_Ser1756=)	rs1554086584

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