{{Rsnum
|rsid=71318369
|Gene=CLCN2
|Chromosome=3
|position=184357688
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=CLCN2
}}{{omim
|id=600570
|rsnum=71318369
|variant=0004
}}{{ClinVar
|rsid=71318369
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=184075476
|CHROM=3
|GMAF=0.0005
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050360000000040116110100
|GENEINFO=CLCN2:1181
|GENE_NAME=CLCN2
|GENE_ID=1181
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.184075476C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600570.0004
|CLNSIG=255
|CLNCUI=CN043197
|CLNDBN=Epilepsy, juvenile myoclonic 8
|Disease=Epilepsy
|CLNACC=RCV000009605.1
|Tags=PM;S3D;SLO;VLD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=MedGen
|CLNDSDBID=CN043197
|COMMON=0
}}