List of variants in gene EIF2AK2 reported as uncertain significance by Baylor Genetics

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_001135651.3(EIF2AK2):c.290C>T (p.Ser97Phe)	rs1573031939
NM_001135651.3(EIF2AK2):c.326C>T (p.Ala109Val)	rs1573031858
NM_001135651.3(EIF2AK2):c.950A>G (p.His317Arg)

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