ClinVar Miner

List of variants in gene APP reported as benign by Genome Diagnostics Laboratory, Amsterdam University Medical Center

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000484.4(APP):c.2124C>T (p.Gly708=)	rs148888161	0.00339
NM_000484.4(APP):c.2212-11_2212-10del	rs112965435	0.00206

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