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rs199472874

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472874(A;A)
Make rs199472874(A;C)
ReferenceGRCh38 38.1/142
Chromosome7
Position150958221
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472874
ebirs199472874
HLIrs199472874
Exacrs199472874
Varsomers199472874
Maprs199472874
PheGenIrs199472874
hapmaprs199472874
1000 genomesrs199472874
hgdprs199472874
ensemblrs199472874
gopubmedrs199472874
geneviewrs199472874
scholarrs199472874
googlers199472874
pharmgkbrs199472874
gwascentralrs199472874
openSNPrs199472874
23andMers199472874
23andMe allrs199472874
SNP Nexus

SNPshotrs199472874
SNPdbers199472874
MSV3drs199472874
GWAS Ctlgrs199472874
Max Magnitude0
ClinVar
Risk rs199472874(A,G;A,G)
Alt rs199472874(A,G;A,G)
Reference rs199472874(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.150655309G>C
CLNSRC ClinVar
CLNACC RCV000058253.2,