{{Rsnum
|rsid=267606926
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=OCLN
|position=68805573
|Gene_s=OCLN
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=C
|CHROM=5
|CLNACC=RCV000007144.1
|CLNALLE=1
|CLNDBN=Band-like calcification with simplified gyration and polymicrogyria
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3489725:251290:1229
|CLNHGVS=NC_000005.9:g.68805573T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=602876.0003
|Disease=Band-like calcification with simplified gyration and polymicrogyria
|FwdALT=C
|FwdREF=T
|GENEINFO=OCLN:100506658
|GENE_ID=100506658
|GENE_NAME=OCLN
|REF=T
|RSPOS=68805573
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606926
}}