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

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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: 5

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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.5177A>G (p.Glu1726Gly)	rs587780598	0.00001
NM_000038.6(APC):c.170A>T (p.Asp57Val)	rs794729227
NM_000038.6(APC):c.391A>G (p.Thr131Ala)	rs1580329587
NM_000038.6(APC):c.5684C>T (p.Thr1895Ile)	rs752605851

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