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rs199472837

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472837(G;G)
Make rs199472837(G;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974891
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472837
ebirs199472837
HLIrs199472837
Exacrs199472837
Varsomers199472837
Maprs199472837
PheGenIrs199472837
hapmaprs199472837
1000 genomesrs199472837
hgdprs199472837
ensemblrs199472837
gopubmedrs199472837
geneviewrs199472837
scholarrs199472837
googlers199472837
pharmgkbrs199472837
gwascentralrs199472837
openSNPrs199472837
23andMers199472837
23andMe allrs199472837
SNP Nexus

SNPshotrs199472837
SNPdbers199472837
MSV3drs199472837
GWAS Ctlgrs199472837
Max Magnitude0
ClinVar
Risk rs199472837(G;G)
Alt rs199472837(G;G)
Reference rs199472837(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.150671979A>C
CLNSRC ClinVar
CLNACC RCV000057884.2,