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rs199472766

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472766(C;C)
Make rs199472766(C;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2585296
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472766
ebirs199472766
HLIrs199472766
Exacrs199472766
Varsomers199472766
Maprs199472766
PheGenIrs199472766
hapmaprs199472766
1000 genomesrs199472766
hgdprs199472766
ensemblrs199472766
gopubmedrs199472766
geneviewrs199472766
scholarrs199472766
googlers199472766
pharmgkbrs199472766
gwascentralrs199472766
openSNPrs199472766
23andMers199472766
23andMe allrs199472766
SNP Nexus

SNPshotrs199472766
SNPdbers199472766
MSV3drs199472766
GWAS Ctlgrs199472766
Max Magnitude0
ClinVar
Risk rs199472766(C;C)
Alt rs199472766(C;C)
Reference rs199472766(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.2606526T>C
CLNSRC ClinVar
CLNACC RCV000057557.2,