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

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.3920T>A (p.Ile1307Lys)	rs1801155	0.00116
NM_000038.6(APC):c.5026A>G (p.Arg1676Gly)	rs370560998	0.00006
NM_000038.6(APC):c.7399C>A (p.Pro2467Thr)	rs372305287	0.00006
NM_000038.6(APC):c.5912C>G (p.Ser1971Cys)	rs754691867	0.00003
NM_000038.6(APC):c.1396A>G (p.Met466Val)	rs781364007	0.00002
NM_000038.6(APC):c.5290C>G (p.Gln1764Glu)	rs529543591	0.00002
NM_000038.6(APC):c.1435T>A (p.Leu479Met)	rs780577693	0.00001
NM_000038.6(APC):c.7778A>G (p.Asn2593Ser)	rs367676584	0.00001
NM_000038.6(APC):c.1703G>T (p.Ser568Ile)	rs962373452

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