{{Rsnum
|rsid = 28928905
|Gene = KCNH2
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=7
|position=150952514
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNH2
}}{{omim
|desc=LONG QT SYNDROME, BRADYCARDIA-INDUCED
|id=152427
|rsnum=28928905
|variant=0011
}}
{{ neighbor
| rsid = 28928904
| distance = 899
}}

{{ClinVar
|rsid=28928905
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=150649602
|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.150649602C>G; NC_000007.13:g.150649602C>T
|CLNORIGIN=1
|CLNSRCID=
152427.0011
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000057911.1; RCV000015511.24; RCV000057910.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDBN=not provided; Long QT syndrome, bradycardia-induced
|CLNSRC=OMIM Allelic Variant
|Disease=not provided; Long QT syndrome
}}

{{PMID Auto
|PMID=19214780
|Title=In silico investigations on functional and haplotype tag SNPs associated with congenital long QT syndromes (LQTSs).
|OA=1
}}

{{PMID Auto
|PMID=11170080
|Title=Bradycardia-induced long QT syndrome caused by a de novo missense mutation in the S2-S3 inner loop of HERG.
}}

{{PMID Auto
|PMID=18441445
|Title=Mutation site dependent variability of cardiac events in Japanese LQT2 form of congenital long-QT syndrome.
}}

{{PMID Auto
|PMID=18808722
|Title=Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations.
|OA=1
}}

{{PMID Auto
|PMID=19716085
|Title=Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.
|OA=1
}}

{{PMID Auto
|PMID=20975234
|Title=Atrioventricular block-induced Torsades de Pointes with clinical and molecular backgrounds similar to congenital long QT syndrome.
}}

{{PMID Auto
|PMID=17560885
|Title=A novel mutation in human ether-a-go-go-related gene, alanine to proline at position 490, found in a large family with autosomal dominant long QT syndrome.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}