List of variants in gene APC reported as benign by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.5465T>A (p.Val1822Asp)	rs459552	0.82099
NM_000038.6(APC):c.5034G>A (p.Gly1678=)	rs42427	0.59504
NM_000038.6(APC):c.5880G>A (p.Pro1960=)	rs465899	0.59308
NM_000038.6(APC):c.5268T>G (p.Ser1756=)	rs866006	0.59230
NM_000038.6(APC):c.4479G>A (p.Thr1493=)	rs41115	0.59177
NM_000038.6(APC):c.1635G>A (p.Ala545=)	rs351771	0.59150
NM_000038.6(APC):c.1458T>C (p.Tyr486=)	rs2229992	0.46792
NM_000038.6(APC):c.136-53T>C	rs2304793	0.07347
NM_000038.6(APC):c.645+32C>T	rs2909961	0.06662
NM_000038.6(APC):c.7704A>G (p.Gly2568=)	rs35043160	0.02992
NM_000038.6(APC):c.220+124C>G	rs76552546	0.01839
NM_000038.6(APC):c.7504G>A (p.Gly2502Ser)	rs2229995	0.01693
NM_000038.6(APC):c.3732A>G (p.Gln1244=)	rs74380081	0.01174
NM_000038.6(APC):c.1695A>G (p.Glu565=)	rs77921116	0.01170
NM_000038.6(APC):c.730-29A>T	rs75083764	0.01144
NM_000038.6(APC):c.7201C>T (p.Leu2401=)	rs2229994	0.01134
NM_000038.6(APC):c.645+61C>T	rs56328836	0.01110
NM_000038.6(APC):c.1627-93A>C	rs115157960	0.00999
NM_000038.6(APC):c.1312+27G>A	rs74975092	0.00973
NM_000038.6(APC):c.422+75T>C	rs112114081	0.00876
NM_000038.6(APC):c.1959G>A (p.Arg653=)	rs72541809	0.00583
NM_000038.6(APC):c.3949G>C (p.Glu1317Gln)	rs1801166	0.00570
NM_000038.6(APC):c.1958+8T>C	rs62626346	0.00510
NM_000038.6(APC):c.729+23T>C	rs75111475	0.00381
NM_000038.6(APC):c.7862C>G (p.Ser2621Cys)	rs72541816	0.00358
NM_000038.6(APC):c.705A>G (p.Leu235=)	rs147036141	0.00213
NM_000038.6(APC):c.423-16A>T	rs78919815	0.00101

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