{{Rsnum
|rsid=121912506
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNH2
|position=150948984
|Gene_s=KCNH2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=152427
|rsnum=121912506
|variant=0005
}}{{ClinVar
|rsid=121912506
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=150646072
|CHROM=7
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=KCNH2:3757
|GENE_NAME=KCNH2
|GENE_ID=3757
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.150646072C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=152427.0005
|CLNSIG=5
|CLNCUI=C1835325
|CLNDBN=Long QT syndrome 2; not provided
|Disease=Long QT syndrome 2; not provided
|CLNACC=RCV000015505.24; RCV000058125.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1129:C3150943:613688:101016
}}{{PMID Auto
|PMID=164320
|Title=Species differences in the hormonal control of lipogenesis in rat and chicken hepatocytes.
}}

{{PMID Auto
|PMID=8914737
|Title=Novel missense mutation in the cyclic nucleotide-binding domain of HERG causes long QT syndrome.
}}

{{PMID Auto
|PMID=10086971
|Title=C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence.
}}

{{PMID Auto
|PMID=11222472
|Title=Notched T waves on Holter recordings enhance detection of patients with LQt2 (HERG) mutations.
}}

{{PMID Auto
|PMID=11854117
|Title=Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel.
}}

{{PMID Auto
|PMID=15840476
|Title=Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.
}}