List of variants reported as uncertain significance for ABetaA21G amyloidosis by Fulgent Genetics, Fulgent Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000484.4(APP):c.47G>A (p.Arg16Gln)	rs955517095	0.00005
NM_000484.4(APP):c.674T>C (p.Val225Ala)	rs746313873	0.00002
NM_000484.4(APP):c.1450C>T (p.Pro484Ser)	rs768238394	0.00001
NM_000484.4(APP):c.-170C>A	rs538664273
NM_000484.4(APP):c.1037C>A (p.Ser346Tyr)	rs1260561215

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