List of variants in gene APP reported as uncertain significance by Department of Pathology and Laboratory Medicine, Sinai Health System

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000484.4(APP):c.982C>T (p.Arg328Trp)	rs200978018	0.00017
NM_000484.4(APP):c.47G>A (p.Arg16Gln)	rs955517095	0.00005
NM_000484.4(APP):c.1012A>G (p.Met338Val)

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