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rs199472898

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472898(C;C)
Make rs199472898(C;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150952703
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472898
ebirs199472898
HLIrs199472898
Exacrs199472898
Varsomers199472898
Maprs199472898
PheGenIrs199472898
hapmaprs199472898
1000 genomesrs199472898
hgdprs199472898
ensemblrs199472898
gopubmedrs199472898
geneviewrs199472898
scholarrs199472898
googlers199472898
pharmgkbrs199472898
gwascentralrs199472898
openSNPrs199472898
23andMers199472898
23andMe allrs199472898
SNP Nexus

SNPshotrs199472898
SNPdbers199472898
MSV3drs199472898
GWAS Ctlgrs199472898
Max Magnitude0
ClinVar
Risk rs199472898(C;C)
Alt rs199472898(C;C)
Reference rs199472898(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.150649791A>G
CLNSRC ClinVar
CLNACC RCV000057883.2,