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rs199472864

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472864(C;T)
Make rs199472864(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150959622
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472864
ebirs199472864
HLIrs199472864
Exacrs199472864
Varsomers199472864
Maprs199472864
PheGenIrs199472864
hapmaprs199472864
1000 genomesrs199472864
hgdprs199472864
ensemblrs199472864
gopubmedrs199472864
geneviewrs199472864
scholarrs199472864
googlers199472864
pharmgkbrs199472864
gwascentralrs199472864
openSNPrs199472864
23andMers199472864
23andMe allrs199472864
SNP Nexus

SNPshotrs199472864
SNPdbers199472864
MSV3drs199472864
GWAS Ctlgrs199472864
Max Magnitude0
ClinVar
Risk rs199472864(T;T)
Alt rs199472864(T;T)
Reference rs199472864(C;C)
Significance Pathogenic
Disease not provided Long QT syndrome not specified
Variation info
Gene KCNH2
CLNDBN not provided Long QT syndrome not specified
Reversed 1
HGVS NC_000007.13:g.150656710G>A
CLNSRC
CLNACC RCV000058233.2, RCV000148539.1, RCV000181756.2,