{{Rsnum
|rsid=137852681
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CLCN2
|position=184352810
|Gene_s=CLCN2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600570
|variant=0003
|rsnum=137852681
}}{{ClinVar
|rsid=137852681
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=184070598
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CLCN2:1181
|GENE_NAME=CLCN2
|GENE_ID=1181
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.184070598C>T
|CLNORIGIN=1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNACC=RCV000009604.2
|CLNDBN=Reclassified - variant of unknown significance
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600570.0003
|Disease=Reclassified - variant of unknown significance
}}