{{Rsnum
|rsid=120074153
|Chromosome=8
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=VPS13B
|position=99784394
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=VPS13B
}}{{omim
|desc=[[Cohen Syndrome]]
|id=607817
|rsnum=120074153
|variant=0007
}}{{ClinVar
|rsid=120074153
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=100796622
|CHROM=8
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=VPS13B:157680
|GENE_NAME=VPS13B
|GENE_ID=157680
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.100796622G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607817.0007
|CLNSIG=5
|CLNCUI=C0265223
|CLNDBN=Cohen syndrome
|Disease=Cohen syndrome
|CLNACC=RCV000002958.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1482:C0265223:216550:193:56604005
}}