List of variants in gene AGO2 reported as uncertain significance by Labcorp Genetics (formerly Invitae), Labcorp

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_012154.5(AGO2):c.227A>G (p.Glu76Gly)
NM_012154.5(AGO2):c.349G>T (p.Val117Phe)	rs1345869518
NM_012154.5(AGO2):c.424G>A (p.Ala142Thr)	rs753058876

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