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rs199472774

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472774(C;C)
Make rs199472774(C;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2587615
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472774
ebirs199472774
HLIrs199472774
Exacrs199472774
Varsomers199472774
Maprs199472774
PheGenIrs199472774
hapmaprs199472774
1000 genomesrs199472774
hgdprs199472774
ensemblrs199472774
gopubmedrs199472774
geneviewrs199472774
scholarrs199472774
googlers199472774
pharmgkbrs199472774
gwascentralrs199472774
openSNPrs199472774
23andMers199472774
23andMe allrs199472774
SNP Nexus

SNPshotrs199472774
SNPdbers199472774
MSV3drs199472774
GWAS Ctlgrs199472774
Max Magnitude0
ClinVar
Risk rs199472774(C;C)
Alt rs199472774(C;C)
Reference rs199472774(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2608845T>C
CLNSRC ClinVar
CLNACC RCV000057568.2,