List of variants in gene combination EIF2AK3, LOC101928371 reported as likely benign by Genetic Services Laboratory, University of Chicago

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_004836.7(EIF2AK3):c.2110G>T (p.Ala704Ser)	rs1805165	0.76783
NM_004836.7(EIF2AK3):c.3153C>T (p.Tyr1051=)	rs56120877	0.00086
NM_004836.7(EIF2AK3):c.2532T>C (p.Ser844=)	rs56094918	0.00039

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