{{Rsnum
|rsid=397514646
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=EIF2B5
|position=184140122
|Gene_s=EIF2B5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=3
|CLNACC=RCV000033200.1
|CLNALLE=1
|CLNDBN=Leukoencephalopathy with vanishing white matter
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1258:C1858991:603896:135
|CLNHGVS=NC_000003.11:g.183857910G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603945.0012
|Disease=Leukoencephalopathy with vanishing white matter
|FwdALT=C
|FwdREF=G
|GENEINFO=EIF2B5:8893
|GENE_ID=8893
|GENE_NAME=EIF2B5
|REF=G
|RSPOS=183857910
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514646
}}