List of variants in gene APC reported as uncertain significance for Colorectal adenoma

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

Total variants: 9

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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.3479C>A (p.Thr1160Lys)	rs201004111	0.00017
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.4732T>G (p.Cys1578Gly)	rs138367627

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