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rs199472852

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472852(G;G)
Make rs199472852(G;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974737
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472852
ebirs199472852
HLIrs199472852
Exacrs199472852
Varsomers199472852
Maprs199472852
PheGenIrs199472852
hapmaprs199472852
1000 genomesrs199472852
hgdprs199472852
ensemblrs199472852
gopubmedrs199472852
geneviewrs199472852
scholarrs199472852
googlers199472852
pharmgkbrs199472852
gwascentralrs199472852
openSNPrs199472852
23andMers199472852
23andMe allrs199472852
SNP Nexus

SNPshotrs199472852
SNPdbers199472852
MSV3drs199472852
GWAS Ctlgrs199472852
Max Magnitude0
ClinVar
Risk rs199472852(G;G)
Alt rs199472852(G;G)
Reference rs199472852(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150671825A>C
CLNSRC ClinVar
CLNACC RCV000058167.2,