{{Rsnum
|rsid=104894583
|Chromosome=17
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=KCNJ2
|position=70175685
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNJ2
}}{{omim
|id=600681
|rsnum=104894583
|variant=0009
}}{{ClinVar
|rsid=104894583
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=68171826
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=KCNJ2:3759
|GENE_NAME=KCNJ2
|GENE_ID=3759
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.68171826A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600681.0009
|CLNSIG=5
|CLNCUI=C1563715
|CLNDBN=Andersen Tawil syndrome; not provided
|Disease=Andersen Tawil syndrome; not provided
|CLNACC=RCV000009481.3; RCV000058324.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1264:C1563715:170390:37553:422348008
}}{{PMID Auto
|PMID=12163457
|Title=Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome).
|OA=1
}}