{{Rsnum
|rsid=180177327
|Chromosome=8
|Orientation=plus
|geno1=(-;-)
|geno2=(-;CT)
|geno3=(CT;CT)
|Gene=VPS13B
|position=99442538
|Gene_s=VPS13B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=180177327
|Reversed=0
|FwdREF=CT
|FwdALT=
|REF=CCT
|ALT=C
|RSPOS=100454763
|CHROM=8
|dbSNPBuildID=135
|SSR=0
|SAO=1
|VP=0x050060000000000002110200
|GENEINFO=VPS13B:157680
|GENE_NAME=VPS13B
|GENE_ID=157680
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.100454766_100454767delCT
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607817.0001
|CLNSIG=5
|CLNCUI=C0265223
|CLNDBN=Cohen syndrome; not provided
|Disease=Cohen syndrome; not provided
|CLNACC=RCV000002952.1; RCV000058939.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1482:C0265223:216550:193:56604005
}}