List of variants in gene APP reported as likely benign for ABetaA21G amyloidosis

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_000484.4(APP):c.1840A>G (p.Ser614Gly)	rs112263157	0.00475
NM_000484.4(APP):c.2124C>T (p.Gly708=)	rs148888161	0.00339
NM_000484.4(APP):c.1458+18C>T	rs200083249
NM_000484.4(APP):c.2148C>T (p.Ile716=)	rs145564988

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