{{Rsnum
|rsid=113994074
|Chromosome=3
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=EIF2B5
|position=184141925
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=EIF2B5
}}{{omim
|id=603945
|rsnum=113994074
|variant=0003
}}{{ClinVar
|rsid=113994074
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=183859713
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=EIF2B5:8893
|GENE_NAME=EIF2B5
|GENE_ID=8893
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.183859713G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=603945.0003
|CLNSIG=5
|CLNCUI=C1858991
|CLNDBN=Leukoencephalopathy with vanishing white matter
|Disease=Leukoencephalopathy with vanishing white matter
|CLNACC=RCV000006307.1
|Tags=PM;PMC;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.
}}