{{Rsnum
|rsid=113994037
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=EIF2B4
|position=27366758
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=EIF2B4
}}{{omim
|id=606687
|rsnum=113994037
|variant=0003
}}{{PMID Auto
|PMID=11835386
|Title=Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter.
}}

{{PMID Auto
|PMID=14572143
|Title=Leukoencephalopathy with vanishing white matter: from magnetic resonance imaging pattern to five genes.
}}{{ClinVar
|ALT=T
|CHROM=2
|CLNACC=RCV000004335.1
|CLNALLE=1
|CLNDBN=Leukoencephalopathy with vanishing white matter
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1258:C1858991:603896:135
|CLNHGVS=NC_000002.11:g.27589625C>T
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606687.0003
|Disease=Leukoencephalopathy with vanishing white matter
|FwdALT=A
|FwdREF=G
|GENEINFO=EIF2B4:8890
|GENE_ID=8890
|GENE_NAME=EIF2B4
|REF=C
|RSPOS=27589625
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=132
|rsid=113994037
}}