List of variants in gene AGO2 reported as benign by Breakthrough Genomics, Breakthrough Genomics

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_012154.5(AGO2):c.1403+9C>G	rs2292779	0.61758
NM_012154.5(AGO2):c.1443C>T (p.Ala481=)	rs2292781	0.40619
NM_012154.5(AGO2):c.1101G>A (p.Ala367=)	rs2271738	0.37389
NM_012154.5(AGO2):c.336+15A>G	rs13276958	0.32450
NM_012154.5(AGO2):c.1890C>T (p.Arg630=)	rs2293939	0.21757
NM_012154.5(AGO2):c.2169+7T>C	rs73713169	0.01160
NM_012154.5(AGO2):c.1533G>A (p.Thr511=)	rs60474948	0.01132
NM_012154.5(AGO2):c.1707C>G (p.Val569=)	rs57810503	0.01067
NM_012154.5(AGO2):c.1929C>T (p.Ala643=)	rs113224509	0.00475

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