ClinVar Miner

List of variants in gene APP reported as likely benign for Early-onset autosomal dominant 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000484.3(APP):c.-156G>C	rs45476095	0.00751
NC_000021.9:g.25880545A>C	rs45599935	0.00601

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