{{Rsnum
|rsid=281875284
|Chromosome=20
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=VAPB
|position=58418289
|Gene_s=VAPB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=20
|CLNACC=RCV000023467.1; RCV000059634.1
|CLNALLE=1
|CLNDBN=Amyotrophic lateral sclerosis type 8; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1450:C1837728:608627:803
|CLNHGVS=NC_000020.10:g.56993345C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNSRCID=605704.0002; VAR_067964
|Disease=Amyotrophic lateral sclerosis type 8; not provided
|FwdALT=T
|FwdREF=C
|REF=C
|RSPOS=56993345
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=281875284
|GENEINFO=VAPB:9217
|GENE_ID=9217
|GENE_NAME=VAPB
}}{{PMID Auto
|PMID=20940299
|Title=Characterization of the properties of a novel mutation in VAPB in familial amyotrophic lateral sclerosis.
|OA=1
}}