{{Rsnum
|rsid=104894426
|Chromosome=14
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=EIF2B2
|position=75009079
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=EIF2B2
}}{{omim
|id=606454
|rsnum=104894426
|variant=0002
}}{{ClinVar
|rsid=104894426
|Reversed=0
|FwdREF=T
|FwdALT=A
|REF=T
|ALT=A
|RSPOS=75475782
|CHROM=14
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=EIF2B2:8892
|GENE_NAME=EIF2B2
|GENE_ID=8892
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.75475782T>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=606454.0002
|CLNSIG=5
|CLNCUI=C1858991
|CLNDBN=Leukoencephalopathy with vanishing white matter
|Disease=Leukoencephalopathy with vanishing white matter
|CLNACC=RCV000004585.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1258:C1858991:603896:135
}}{{PMID Auto
|PMID=11704758
|Title=Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter.
}}

{{PMID Auto
|PMID=14572143
|Title=Leukoencephalopathy with vanishing white matter: from magnetic resonance imaging pattern to five genes.
}}