List of variants in gene EIF2B1 reported as benign for Vanishing white matter disease

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001414.4(EIF2B1):c.*464A>G	rs9919	0.40370
NM_001414.4(EIF2B1):c.*395T>C	rs1050449	0.30842
NM_001414.3(EIF2B1):c.-144G>C	rs34827093	0.07765
NM_001414.4(EIF2B1):c.*731T>C	rs10846532	0.07470
NM_001414.4(EIF2B1):c.*665C>T	rs2707	0.07425
NM_001414.4(EIF2B1):c.*426G>C	rs113041500	0.01648
NM_001414.4(EIF2B1):c.417A>G (p.Glu139=)	rs73414297	0.00961

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