List of variants in gene combination APP, APP-DT reported as likely benign for Alzheimer disease

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
NC_000021.9:g.26171246G>A	rs139885956	0.00230
NC_000021.9:g.26171301C>T	rs187510057	0.00096

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