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rs199472869

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472869(A;G)
Make rs199472869(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150958323
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472869
ebirs199472869
HLIrs199472869
Exacrs199472869
Varsomers199472869
Maprs199472869
PheGenIrs199472869
hapmaprs199472869
1000 genomesrs199472869
hgdprs199472869
ensemblrs199472869
gopubmedrs199472869
geneviewrs199472869
scholarrs199472869
googlers199472869
pharmgkbrs199472869
gwascentralrs199472869
openSNPrs199472869
23andMers199472869
23andMe allrs199472869
SNP Nexus

SNPshotrs199472869
SNPdbers199472869
MSV3drs199472869
GWAS Ctlgrs199472869
Max Magnitude0
ClinVar
Risk rs199472869(G;G)
Alt rs199472869(G;G)
Reference rs199472869(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150655411T>C
CLNSRC ClinVar
CLNACC RCV000058245.2,