{{Rsnum
|rsid=104894584
|Chromosome=17
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNJ2
|position=70175553
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNJ2
}}{{omim
|id=600681
|rsnum=104894584
|variant=0010
}}{{ClinVar
|rsid=104894584
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=68171694
|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.68171694G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600681.0010
|CLNSIG=5
|CLNCUI=C1865018
|CLNDBN=Short QT syndrome 3; not provided
|Disease=Short QT syndrome 3; not provided
|CLNACC=RCV000009482.1; RCV000058318.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1865018:609622:51083
}}{{PMID Auto
|PMID=15761194
|Title=A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.
}}