{{Rsnum
|rsid=386834105
|Chromosome=8
|position=99766869
|Orientation=plus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=VPS13B
|Gene_s=VPS13B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=8
|CLNACC=RCV000050099.1
|CLNALLE=1
|CLNDBN=Cohen syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1482:C0265223:216550:193:56604005
|CLNHGVS=NC_000008.10:g.100779097delG
|CLNSIG=4
|Disease=Cohen syndrome
|FwdREF=G
|REF=AG
|RSPOS=100779096
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386834105
|GENEINFO=VPS13B:157680
|GENE_ID=157680
|GENE_NAME=VPS13B
}}{{PMID Auto
|PMID=15173253
|Title=Broader geographical spectrum of Cohen syndrome due to COH1 mutations.
|OA=1
}}