{{Rsnum
|rsid=104894579
|Chromosome=17
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=KCNJ2
|position=70175938
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNJ2
}}{{omim
|id=600681
|rsnum=104894579
|variant=0003
}}{{ClinVar
|rsid=104894579
|Reversed=0
|FwdREF=G
|FwdALT=A,C,T
|REF=G
|ALT=A,C,T
|RSPOS=68172079
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110104
|GENEINFO=KCNJ2:3759
|GENE_NAME=KCNJ2
|GENE_ID=3759
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000017.10:g.68172079G>A; NC_000017.10:g.68172079G>C; NC_000017.10:g.68172079G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600681.0003
|CLNSIG=5
|CLNCUI=C1563715
|CLNDBN=not provided; Andersen Tawil syndrome
|Disease=not provided; Andersen Tawil syndrome
|CLNACC=RCV000058330.1; RCV000058331.1; RCV000009475.1; RCV000058332.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1264:C1563715:170390:37553:422348008
}}{{PMID Auto
|PMID=21640645
|Title=Unique post-exercise electrophysiological test results in a new Andersen-Tawil syndrome mutation.
}}

{{PMID Auto
|PMID=12796536
|Title=PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome.
}}

{{PMID Auto
|PMID=15831539
|Title=In vivo and in vitro functional characterization of Andersen's syndrome mutations.
|OA=1
}}

{{PMID Auto
|PMID=16217063
|Title=Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variation.
}}

{{PMID Auto
|PMID=11371347
|Title=Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome.
}}

{{PMID Auto
|PMID=12163457
|Title=Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome).
|OA=1
}}

{{PMID Auto
|PMID=17221872
|Title=Genotype-phenotype correlations of KCNJ2 mutations in Japanese patients with Andersen-Tawil syndrome.
}}