ClinVar Miner

List of variants in gene EIF2AK2 reported as uncertain significance by Undiagnosed Diseases Network, NIH

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001135651.3(EIF2AK2):c.31A>C (p.Met11Leu)	rs1363544084
NM_001135651.3(EIF2AK2):c.398A>T (p.Tyr133Phe)	rs1573029592

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