List of variants in gene APC reported as uncertain significance for bile duct neoplasm

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.8332G>T (p.Ala2778Ser)	rs587778046	0.00006
NM_000038.6(APC):c.4440G>C (p.Gln1480His)	rs876659881
NM_000038.6(APC):c.4658C>T (p.Ala1553Val)	rs1554086050
NM_000038.6(APC):c.8461G>A (p.Asp2821Asn)	rs1554089164

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