{{Rsnum
|rsid=121912507
|Chromosome=7
|position=150951511
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNH2
|Gene_s=KCNH2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=152427
|rsnum=121912507
|variant=0008
}}{{ClinVar
|rsid=121912507
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=150648599
|CHROM=7
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=KCNH2:3757
|GENE_NAME=KCNH2
|GENE_ID=3757
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.150648599C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=152427.0008
|CLNSIG=5
|CLNCUI=C1835325
|CLNDBN=Long QT syndrome 2; not provided
|Disease=Long QT syndrome 2; not provided
|CLNACC=RCV000015508.24; RCV000058029.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1129:C3150943:613688:101016
}}{{PMID Auto
|PMID=163795
|Title=Response of irradiated mice to live-virus (TC-83) immunization.
|OA=1
}}

{{PMID Auto
|PMID=7889573
|Title=A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome.
}}

{{PMID Auto
|PMID=10973849
|Title=Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.
}}

{{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=14998624
|Title=Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations.
}}

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