List of variants in gene SERPINA1 reported as uncertain significance by GeneDx

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000295.5(SERPINA1):c.922G>T (p.Ala308Ser)	rs141620200	0.00215
NM_001127701.1(SERPINA1):c.739C>T (p.Arg247Cys)	rs28929470	0.00199
NM_000295.5(SERPINA1):c.976G>A (p.Val326Ile)	rs139964603	0.00078
NM_000295.5(SERPINA1):c.43C>T (p.Leu15=)	rs147283849	0.00061
NM_000295.4(SERPINA1):c.1078G>A (p.Ala360Thr)	rs1802959	0.00001
NM_000295.5(SERPINA1):c.700G>A (p.Val234Met)	rs374168370	0.00001
NM_000295.5(SERPINA1):c.880G>A (p.Asp294Asn)	rs772436715	0.00001
NM_000295.5(SERPINA1):c.1045G>C (p.Ala349Pro)
NM_000295.5(SERPINA1):c.1070T>C (p.Val357Ala)	rs1595598934

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