List of variants studied for colorectal adenoma

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.4420G>A (p.Ala1474Thr)	rs139387758	0.00324
NM_000038.6(APC):c.4360A>G (p.Lys1454Glu)	rs111866410	0.00271
NM_000038.6(APC):c.4336G>A (p.Ala1446Thr)	rs146572883	0.00056
NM_000038.6(APC):c.2847G>T (p.Met949Ile)	rs147394539	0.00039
NM_000038.6(APC):c.8266A>G (p.Ile2756Val)	rs146115809	0.00026
NM_000038.6(APC):c.4237A>G (p.Met1413Val)	rs141519952	0.00018
NM_000038.6(APC):c.3479C>A (p.Thr1160Lys)	rs201004111	0.00017
NM_000038.6(APC):c.6985A>G (p.Ile2329Val)	rs146048493	0.00015
NM_000038.6(APC):c.7717A>G (p.Ile2573Val)	rs145444830	0.00007
NM_000038.6(APC):c.449A>G (p.Lys150Arg)	rs371085910	0.00004
NM_000038.6(APC):c.8383G>A (p.Ala2795Thr)	rs369264968	0.00003
NM_002691.4(POLD1):c.367C>T (p.Pro123Ser)	rs761127022	0.00002
NM_000038.6(APC):c.7778A>G (p.Asn2593Ser)	rs367676584	0.00001
NM_000038.6(APC):c.3927_3931del (p.Glu1309fs)	rs121913224
NM_000038.6(APC):c.4732T>G (p.Cys1578Gly)	rs138367627
NM_000038.6(APC):c.4901del (p.Pro1634fs)	rs1057518901

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