ClinVar Miner

List of variants in gene combination EIF2B3, LOC129930429 reported as benign for leukoencephalopathy with vanishing white matter 1

Included ClinVar conditions (4):

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_020365.5(EIF2B3):c.-72C>G	rs489676

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