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rs199472891

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472891(A;A)
Make rs199472891(A;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150952783
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472891
ebirs199472891
HLIrs199472891
Exacrs199472891
Varsomers199472891
Maprs199472891
PheGenIrs199472891
hapmaprs199472891
1000 genomesrs199472891
hgdprs199472891
ensemblrs199472891
gopubmedrs199472891
geneviewrs199472891
scholarrs199472891
googlers199472891
pharmgkbrs199472891
gwascentralrs199472891
openSNPrs199472891
23andMers199472891
23andMe allrs199472891
SNP Nexus

SNPshotrs199472891
SNPdbers199472891
MSV3drs199472891
GWAS Ctlgrs199472891
Max Magnitude0
ClinVar
Risk rs199472891(A;A)
Alt rs199472891(A;A)
Reference rs199472891(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.150649871A>T
CLNSRC ClinVar
CLNACC RCV000057872.2,