{{Rsnum
|rsid=199473387
|Chromosome=17
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=KCNJ2
|position=70175952
|Gene_s=KCNJ2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C,G
|CHROM=17
|CLNACC=RCV000023028.3; RCV000058335.1; RCV000058336.1
|CLNALLE=1; 2
|CLNDBN=Andersen Tawil syndrome; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1264:C1563715:170390:37553:422348008
|CLNHGVS=NC_000017.10:g.68172093A>C; NC_000017.10:g.68172093A>G
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600681.0013
|Disease=Andersen Tawil syndrome; not provided
|FwdALT=C,G
|FwdREF=A
|GENEINFO=KCNJ2:3759
|GENE_ID=3759
|GENE_NAME=KCNJ2
|REF=A
|RSPOS=68172093
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000000002100100
|WGT=0
|dbSNPBuildID=136
|rsid=199473387
}}{{PMID Auto
|PMID=17324964
|Title=Corticosteroid-exacerbated symptoms in an Andersen's syndrome kindred.
}}

{{PMID Auto
|PMID=17341397
|Title=KCNJ2 mutations in arrhythmia patients referred for LQT testing: a mutation T305A with novel effect on rectification properties.
|OA=1
}}