List of variants reported as likely benign by ClinGen InSiGHT Hereditary Colorectal Cancer/Polyposis Variant Curation Expert Panel

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.1487C>T (p.Thr496Ile)	rs1369979539	0.00001
NM_000038.6(APC):c.4906G>T (p.Asp1636Tyr)	rs730882128	0.00001
NM_000038.6(APC):c.123A>G (p.Ala41=)	rs1561445056
NM_000038.6(APC):c.235A>G (p.Ser79Gly)	rs1001856924
NM_000038.6(APC):c.420G>C (p.Glu140Asp)	rs202161017
NM_000038.6(APC):c.645+9C>A	rs863224286
NM_000038.6(APC):c.8438C>A (p.Thr2813Lys)	rs1060503275

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