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rs199472899

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472899(C;T)
Make rs199472899(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150952699
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472899
ebirs199472899
HLIrs199472899
Exacrs199472899
Varsomers199472899
Maprs199472899
PheGenIrs199472899
hapmaprs199472899
1000 genomesrs199472899
hgdprs199472899
ensemblrs199472899
gopubmedrs199472899
geneviewrs199472899
scholarrs199472899
googlers199472899
pharmgkbrs199472899
gwascentralrs199472899
openSNPrs199472899
23andMers199472899
23andMe allrs199472899
SNP Nexus

SNPshotrs199472899
SNPdbers199472899
MSV3drs199472899
GWAS Ctlgrs199472899
Max Magnitude0
ClinVar
Risk rs199472899(T;T)
Alt rs199472899(T;T)
Reference rs199472899(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.150649787G>A
CLNSRC ClinVar
CLNACC RCV000057887.2,