List of variants in gene EEF1A2 reported as benign by Athena Diagnostics Inc

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001958.5(EEF1A2):c.594T>C (p.Gly198=)	rs310617	0.57688
NM_001958.5(EEF1A2):c.1326G>A (p.Glu442=)	rs1042796	0.04304
NM_001958.5(EEF1A2):c.207C>T (p.Arg69=)	rs3818681	0.03482
NM_001958.5(EEF1A2):c.1263C>T (p.Leu421=)	rs115107511	0.00453
NM_001958.5(EEF1A2):c.1030-8G>A	rs112283537	0.00314
NM_001958.5(EEF1A2):c.1296G>A (p.Thr432=)	rs200259257	0.00299
NM_001958.5(EEF1A2):c.1266C>A (p.Gly422=)	rs202102758	0.00277
NM_001958.5(EEF1A2):c.54C>G (p.Ser18=)	rs200759764

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