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rs199472998

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472998(G;T)
Make rs199472998(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150950168
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472998
ebirs199472998
HLIrs199472998
Exacrs199472998
Varsomers199472998
Maprs199472998
PheGenIrs199472998
hapmaprs199472998
1000 genomesrs199472998
hgdprs199472998
ensemblrs199472998
gopubmedrs199472998
geneviewrs199472998
scholarrs199472998
googlers199472998
pharmgkbrs199472998
gwascentralrs199472998
openSNPrs199472998
23andMers199472998
23andMe allrs199472998
SNP Nexus

SNPshotrs199472998
SNPdbers199472998
MSV3drs199472998
GWAS Ctlgrs199472998
Max Magnitude0
ClinVar
Risk rs199472998(T;T)
Alt rs199472998(T;T)
Reference rs199472998(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150647256C>A
CLNSRC ClinVar
CLNACC RCV000058115.2,