{{Rsnum
|rsid=386834073
|Chromosome=8
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=VPS13B
|position=99147839
|Gene_s=VPS13B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=8
|CLNACC=RCV000050061.1
|CLNALLE=1
|CLNDBN=Cohen syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1482:C0265223:216550:193:56604005
|CLNHGVS=NC_000008.10:g.100160067A>G
|CLNSIG=4
|Disease=Cohen syndrome
|FwdALT=G
|FwdREF=A
|REF=A
|RSPOS=100160067
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386834073
|GENEINFO=VPS13B:157680
|GENE_ID=157680
|GENE_NAME=VPS13B
}}{{PMID Auto
|PMID=20461111
|Title=High frequency of COH1 intragenic deletions and duplications detected by MLPA in patients with Cohen syndrome.
|OA=1
}}