List of variants reported as likely benign for Alzheimer disease by Illumina Laboratory Services, Illumina

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000484.4(APP):c.*590C>A	rs45455403	0.00936
NM_000484.4(APP):c.2124C>T (p.Gly708=)	rs148888161	0.00348
NM_000484.4(APP):c.*372A>G	rs187940037	0.00231
NM_000484.4(APP):c.1795G>A (p.Glu599Lys)	rs140304729	0.00143
NM_000484.4(APP):c.*624A>G	rs199680232	0.00100
NM_000484.4(APP):c.-44C>T	rs200289921	0.00093
NM_000484.4(APP):c.1305C>T (p.Phe435=)	rs148180403	0.00069
NM_000484.4(APP):c.592T>C (p.Ser198Pro)	rs145081708	0.00043
NM_000484.4(APP):c.355+9G>A	rs371324252	0.00013
NM_000484.4(APP):c.*738T>C	rs201621005	0.00012
NM_000484.4(APP):c.225+14G>A	rs199644062	0.00011
NM_000484.4(APP):c.704C>T (p.Ala235Val)	rs139819006	0.00006
NM_000484.4(APP):c.*663C>T	rs572356515	0.00003

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