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rs199472706

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472706(C;T)
Make rs199472706(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2571391
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472706
ebirs199472706
HLIrs199472706
Exacrs199472706
Varsomers199472706
Maprs199472706
PheGenIrs199472706
hapmaprs199472706
1000 genomesrs199472706
hgdprs199472706
ensemblrs199472706
gopubmedrs199472706
geneviewrs199472706
scholarrs199472706
googlers199472706
pharmgkbrs199472706
gwascentralrs199472706
openSNPrs199472706
23andMers199472706
23andMe allrs199472706
SNP Nexus

SNPshotrs199472706
SNPdbers199472706
MSV3drs199472706
GWAS Ctlgrs199472706
Max Magnitude0
ClinVar
Risk rs199472706(T;T)
Alt rs199472706(T;T)
Reference rs199472706(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2592621C>T
CLNSRC ClinVar
CLNACC RCV000057729.2,