{{Rsnum
|rsid=74315431
|Chromosome=20
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=VAPB
|position=58418318
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=VAPB
}}{{omim
|id=605704
|rsnum=74315431
|variant=0001
}}{{ClinVar
|rsid=74315431
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=56993374
|CHROM=20
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=VAPB:9217
|GENE_NAME=VAPB
|GENE_ID=9217
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.56993374C>T
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=605704.0001; VAR_026743
|CLNSIG=5
|CLNCUI=C1837728
|CLNDBN=Amyotrophic lateral sclerosis type 8; Spinal muscular atrophy, late-onset, finkel type; Amyotrophic lateral sclerosis, typical; not provided
|Disease=Amyotrophic lateral sclerosis type 8; Spinal muscular atrophy; Amyotrophic lateral sclerosis; not provided
|CLNACC=RCV000005073.2; RCV000005074.2; RCV000005075.2; RCV000059635.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1450:C1837728:608627:803; C1854058
}}{{PMID Auto
|PMID=15372378
|Title=A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis.
|OA=1
}}