ClinVar Miner

List of variants in gene combination EIF2AK3, LOC101928371 reported as likely benign by Genome Diagnostics Laboratory, The Hospital for Sick Children

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004836.7(EIF2AK3):c.3291A>G (p.Ser1097=)	rs10208681	0.00543
NM_004836.7(EIF2AK3):c.2532T>C (p.Ser844=)	rs56094918	0.00039

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