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rs199472910

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472910(C;T)
Make rs199472910(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150952508
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472910
ebirs199472910
HLIrs199472910
Exacrs199472910
Varsomers199472910
Maprs199472910
PheGenIrs199472910
hapmaprs199472910
1000 genomesrs199472910
hgdprs199472910
ensemblrs199472910
gopubmedrs199472910
geneviewrs199472910
scholarrs199472910
googlers199472910
pharmgkbrs199472910
gwascentralrs199472910
openSNPrs199472910
23andMers199472910
23andMe allrs199472910
SNP Nexus

SNPshotrs199472910
SNPdbers199472910
MSV3drs199472910
GWAS Ctlgrs199472910
Max Magnitude0
ClinVar
Risk rs199472910(T;T)
Alt rs199472910(T;T)
Reference rs199472910(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150649596G>A
CLNSRC ClinVar
CLNACC RCV000057913.2,