Have questions? Visit https://www.reddit.com/r/SNPedia

rs199472882

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472882(C;T)
Make rs199472882(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150958086
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472882
ebirs199472882
HLIrs199472882
Exacrs199472882
Varsomers199472882
Maprs199472882
PheGenIrs199472882
hapmaprs199472882
1000 genomesrs199472882
hgdprs199472882
ensemblrs199472882
gopubmedrs199472882
geneviewrs199472882
scholarrs199472882
googlers199472882
pharmgkbrs199472882
gwascentralrs199472882
openSNPrs199472882
23andMers199472882
23andMe allrs199472882
SNP Nexus

SNPshotrs199472882
SNPdbers199472882
MSV3drs199472882
GWAS Ctlgrs199472882
Max Magnitude0
ClinVar
Risk rs199472882(T;T)
Alt rs199472882(T;T)
Reference rs199472882(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150655174G>A
CLNSRC ClinVar
CLNACC RCV000058269.2, RCV000181771.1,