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rs36210421

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs36210421(G;T)
Make rs36210421(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947340
GeneKCNH2
is asnp
is mentioned by
dbSNPrs36210421
ebirs36210421
HLIrs36210421
Exacrs36210421
Varsomers36210421
Maprs36210421
PheGenIrs36210421
hapmaprs36210421
1000 genomesrs36210421
hgdprs36210421
ensemblrs36210421
gopubmedrs36210421
geneviewrs36210421
scholarrs36210421
googlers36210421
pharmgkbrs36210421
gwascentralrs36210421
openSNPrs36210421
23andMers36210421
23andMe allrs36210421
SNP Nexus

SNPshotrs36210421
SNPdbers36210421
MSV3drs36210421
GWAS Ctlgrs36210421
GMAF0.01699
Max Magnitude0



ClinVar
Risk rs36210421(T;T)
Alt rs36210421(T;T)
Reference rs36210421(G;G)
Significance Probable-non-pathogenic
Disease Cardiac arrhythmia not provided Torsades de pointes Sudden unexplained death Long QT syndrome 2
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia not provided Torsades de pointes Sudden unexplained death Long QT syndrome 2
Reversed 1
HGVS NC_000007.13:g.150644428C>A
CLNSRC Centenary Institute
CLNACC RCV000030101.1, RCV000058202.2, RCV000171814.2, RCV000172896.1, RCV000203011.1,



[PMID 19019189OA-icon.png] Common candidate gene variants are associated with QT interval duration in the general population.


[PMID 19214780OA-icon.png] In silico investigations on functional and haplotype tag SNPs associated with congenital long QT syndromes (LQTSs).


[PMID 17210] [Carbogen therapy of acute cochlear disorders].


[PMID 14661677] Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome.


[PMID 16487223OA-icon.png] Genetic polymorphisms in KCNQ1, HERG, KCNE1 and KCNE2 genes in the Chinese, Malay and Indian populations of Singapore.


[PMID 17161064] Association of torsades de pointes with novel and known single nucleotide polymorphisms in long QT syndrome genes.


[PMID 17275752] Torsades de pointes complicating atrioventricular block: evidence for a genetic predisposition.


[PMID 11468227] Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome.