List of variants in gene SERPINA1 reported as likely benign by Illumina Laboratory Services, Illumina

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001127701.1(SERPINA1):c.*1703C>T	rs877081	0.11366
NM_000295.5(SERPINA1):c.*1331G>A	rs11568814	0.07789
NM_000295.4(SERPINA1):c.-223A>G	rs55967149	0.03970
NM_000295.5(SERPINA1):c.840T>C (p.Asp280=)	rs1049800	0.03703
NM_000295.5(SERPINA1):c.*1555C>T	rs56325294	0.03636
NM_000295.5(SERPINA1):c.774G>A (p.Lys258=)	rs34112109	0.01536
NM_000295.5(SERPINA1):c.*326A>G	rs7144409	0.01528
NM_000295.5(SERPINA1):c.1068C>T (p.Ala356=)	rs9630	0.00897
NM_000295.4(SERPINA1):c.-208C>T	rs55973910	0.00679
NM_001127701.1(SERPINA1):c.739C>T (p.Arg247Cys)	rs28929470	0.00211

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