{{Rsnum
|rsid = 28937596
|Gene = EIF2B5
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=C
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=3
|position=184144111
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=EIF2B5
}}{{omim
|desc=LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER
|id=603945
|rsnum=28937596
|variant=0002
}}

{{ neighbor
| rsid = 843358
| distance = 656
}}

{{ClinVar
|rsid=28937596
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=183861899
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=EIF2B5:8893
|GENE_NAME=EIF2B5
|GENE_ID=8893
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.183861899T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603945.0002
|CLNSIG=5
|CLNCUI=C1858991
|CLNDBN=Leukoencephalopathy with vanishing white matter
|Disease=Leukoencephalopathy with vanishing white matter
|CLNACC=RCV000006306.1
|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.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}