List of variants in gene APC reported as benign by Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.7504G>A (p.Gly2502Ser)	rs2229995	0.01693
NM_001127511.3(APC):c.78C>A (p.Ser26Arg)	rs113782655	0.00928
NM_000038.6(APC):c.1959G>A (p.Arg653=)	rs72541809	0.00583
NM_000038.6(APC):c.3165A>T (p.Ile1055=)	rs61734287	0.00286
NM_000038.6(APC):c.3511C>T (p.Arg1171Cys)	rs201830995	0.00028
NM_000038.6(APC):c.3462AGA[2] (p.Glu1157del)	rs386833391

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