{{Rsnum
|rsid=104894021
|Chromosome=7
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=KCNH2
|position=150951629
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNH2
}}{{omim
|id=152427
|rsnum=104894021
|variant=0018
}}
{{omim
|id=152427
|rsnum=104894021
|variant=0017
}}{{ClinVar
|rsid=104894021
|Reversed=1
|FwdREF=C
|FwdALT=A,G
|REF=G
|ALT=C,T
|RSPOS=150648717
|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; 2
|CLNHGVS=NC_000007.13:g.150648717G>C; NC_000007.13:g.150648717G>T
|CLNORIGIN=1
|CLNSRCID=
152427.0017; 152427.0018
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000015517.24; RCV000057981.1; RCV000015518.20; RCV000057980.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDBN=Short QT syndrome 1; not provided
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1865020:609620:51083
|CLNSRC=OMIM Allelic Variant
|Disease=Short QT syndrome 1; not provided
}}{{PMID Auto
|PMID=14676148
|Title=Sudden death associated with short-QT syndrome linked to mutations in HERG.
}}

{{PMID Auto
|PMID=15828882
|Title=Short QT syndrome and atrial fibrillation caused by mutation in KCNH2.
}}

{{PMID Auto
|PMID=19088443
|Title=Biophysical characterization of the short QT mutation hERG-N588K reveals a mixed gain-and loss-of-function.
}}

{{PMID Auto
|PMID=19439805
|Title=Comparative effects of the short QT N588K mutation at 37 degrees C on hERG K+ channel current during ventricular, Purkinje fibre and atrial action potentials: an action potential clamp study.
}}

{{PMID Auto
|PMID=19501051
|Title=hERG1a/1b heteromeric currents exhibit amplified attenuation of inactivation in variant 1 short QT syndrome.
|OA=1
}}