List of variants reported as likely benign for familial adenomatous polyposis 1 by Mendelics

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Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.1959G>A (p.Arg653=)	rs72541809	0.00583
NM_000038.6(APC):c.-19+45G>A	rs370011472	0.00550
NM_000038.6(APC):c.933+30A>G	rs145211300	0.00412
NM_000038.6(APC):c.7862C>G (p.Ser2621Cys)	rs72541816	0.00358
NM_000038.6(APC):c.3386T>C (p.Leu1129Ser)	rs143638171	0.00250
NM_000038.6(APC):c.423-17T>A	rs534684461	0.00114
NM_000038.6(APC):c.7514G>A (p.Arg2505Gln)	rs147549623	0.00093
NM_000038.6(APC):c.835-24A>T	rs200399868	0.00091
NM_000038.6(APC):c.6821C>T (p.Ala2274Val)	rs34919187	0.00088
NM_000038.6(APC):c.295C>T (p.Arg99Trp)	rs139196838	0.00048
NM_000038.6(APC):c.2805C>T (p.Tyr935=)	rs137854575	0.00040
NM_000038.6(APC):c.607C>G (p.Gln203Glu)	rs141576417	0.00034
NM_000038.6(APC):c.2232T>G (p.Ser744=)	rs145751759	0.00032
NM_000038.6(APC):c.3511C>T (p.Arg1171Cys)	rs201830995	0.00028
NM_000038.6(APC):c.4237A>G (p.Met1413Val)	rs141519952	0.00018
NM_000038.6(APC):c.6510A>C (p.Pro2170=)	rs138571760	0.00016
NM_000038.6(APC):c.6609T>C (p.Val2203=)	rs149328018	0.00014
NM_000038.6(APC):c.450A>G (p.Lys150=)	rs116020626	0.00012
NM_000038.6(APC):c.-43A>C	rs879254014	0.00011
NM_000038.6(APC):c.388A>G (p.Ser130Gly)	rs150973053	0.00010
NM_000038.6(APC):c.1966C>G (p.Leu656Val)	rs577466163	0.00003
NM_000038.6(APC):c.3225T>C (p.Tyr1075=)	rs768123840	0.00002
NM_000038.6(APC):c.-19+416C>T	rs976627265	0.00001
NM_000038.6(APC):c.2472A>T (p.Pro824=)	rs746965994	0.00001
NM_000038.6(APC):c.3804A>G (p.Pro1268=)	rs878853442	0.00001
NM_000038.6(APC):c.8524T>G (p.Ser2842Ala)	rs587780610	0.00001
NM_001127511.3(APC):c.30C>A (p.Val10=)	rs917976853	0.00001
NM_000038.6(APC):c.409_414dup	rs397817775
NM_000038.6(APC):c.7089A>G (p.Lys2363=)	rs864622761

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