List of variants in gene APC reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.7504G>A (p.Gly2502Ser)	rs2229995	0.01693
NM_000038.6(APC):c.7201C>T (p.Leu2401=)	rs2229994	0.01134
NM_000038.6(APC):c.2608C>T (p.Pro870Ser)	rs33974176	0.00917
NM_000038.6(APC):c.4326T>A (p.Pro1442=)	rs67622085	0.00705
NM_000038.6(APC):c.1959G>A (p.Arg653=)	rs72541809	0.00583
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.607C>G (p.Gln203Glu)	rs141576417	0.00034
NM_000038.6(APC):c.6985A>G (p.Ile2329Val)	rs146048493	0.00015
NM_001127511.3(APC):c.-109C>G	rs761634030	0.00013
NM_000038.6(APC):c.1744-687_1744-686del	rs35769203
NM_000038.6(APC):c.423-17dup	rs35031194
NM_001127511.3(APC):c.-134_-133insG	rs1561393341

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