{{Rsnum
|rsid=398122387
|Chromosome=1
|Orientation=plus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=CNTN2
|position=205059099
|Gene_s=CNTN2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=1
|CLNACC=RCV000054805.18
|CLNALLE=1
|CLNDBN=Epilepsy, familial adult myoclonic, 5
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN179855:615400:ORPHA86814
|CLNHGVS=NC_000001.11:g.205059099delG
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_005076.3:c.503delG; 190197.0001
|Disease=Epilepsy
|FwdREF=G
|GENEINFO=CNTN2:6900
|GENE_ID=6900
|GENE_NAME=CNTN2
|REF=TG
|RSPOS=205059098
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;NSF;REF;ASP;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060001205000002110200
|WGT=1
|dbSNPBuildID=138
|rsid=398122387
|CLNORIGIN=1
}}