ClinVar Miner

List of variants reported as uncertain significance for Vanishing white matter disease by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_020365.5(EIF2B3):c.71C>T (p.Pro24Leu)	rs151320540	0.00017
NM_014239.4(EIF2B2):c.119G>C (p.Gly40Ala)	rs139325888	0.00008

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