{{Rsnum
|rsid=199830292
|Gene=KCNJ5
|Chromosome=11
|position=128916630
|Orientation=plus
|GMAF=0.0004591
|Gene_s=KCNJ5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ClinVar
|ALT=C
|CAF=0.9995; 0.0004591
|CHROM=11
|CLNACC=RCV000009405.1
|CLNALLE=1
|CLNDBN=Long QT syndrome 13
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1129:C3150733:613485:101016
|CLNHGVS=NC_000011.9:g.128786525G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600734.0001
|COMMON=0
|Disease=Long QT syndrome 13
|FwdALT=C
|FwdREF=G
|GENEINFO=KCNJ5:3762
|GENE_ID=3762
|GENE_NAME=KCNJ5
|REF=G
|RSPOS=128786525
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000016110100
|WGT=0
|dbSNPBuildID=137
|rsid=199830292
}}