{{Rsnum
|rsid=147750704
|Chromosome=17
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNJ2
|position=70175316
|Gene_s=KCNJ2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=17
|CLNACC=RCV000023029.1; RCV000058307.1
|CLNALLE=1
|CLNDBN=Atrial fibrillation, familial, 9; not provided
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3151431:613980
|CLNHGVS=NC_000017.10:g.68171457G>A
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600681.0014
|Disease=Atrial fibrillation; not provided
|FwdALT=A
|FwdREF=G
|GENEINFO=KCNJ2:3759
|GENE_ID=3759
|GENE_NAME=KCNJ2
|REF=G
|RSPOS=68171457
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000000002100100
|WGT=0
|dbSNPBuildID=134
|rsid=147750704
}}{{PMID Auto
|PMID=15922306
|Title=A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation.
}}

{{PMID Auto
|PMID=19041665
|Title=Atrial proarrhythmia due to increased inward rectifier current (I(K1)) arising from KCNJ2 mutation--a simulation study.
}}