List of variants reported as uncertain significance for Alpha-1-antitrypsin deficiency by Fulgent Genetics, Fulgent Genetics

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000295.5(SERPINA1):c.-7A>G	rs559054925	0.00041
NM_000295.5(SERPINA1):c.250G>A (p.Ala84Thr)	rs111850950	0.00031
NM_000295.5(SERPINA1):c.1061C>T (p.Ser354Phe)	rs201788603	0.00021
NM_000295.5(SERPINA1):c.244G>A (p.Ala82Thr)	rs113817720	0.00011
NM_000295.5(SERPINA1):c.1075A>G (p.Lys359Glu)	rs200945035	0.00007
NM_001127701.1(SERPINA1):c.326C>T (p.Thr109Met)	rs199422213	0.00006
NM_000295.5(SERPINA1):c.113C>T (p.Ser38Phe)	rs745463238	0.00004
NM_001127701.1(SERPINA1):c.17C>T (p.Ser6Leu)	rs140814100	0.00004
NM_000295.5(SERPINA1):c.701T>A (p.Val234Glu)	rs746197812	0.00002

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