List of variants in gene APP reported as likely pathogenic 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000484.4(APP):c.2137G>A (p.Ala713Thr)	rs63750066	0.00006
NM_000484.4(APP):c.2125G>A (p.Gly709Ser)	rs201269325	0.00003
NM_000484.4(APP):c.2059A>C (p.Lys687Gln)
NM_000484.4(APP):c.2061A>C (p.Lys687Asn)
NM_000484.4(APP):c.2113C>G (p.Leu705Val)	rs63750921

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