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rs199472711

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472711(G;G)
Make rs199472711(G;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2572051
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472711
ebirs199472711
HLIrs199472711
Exacrs199472711
Varsomers199472711
Maprs199472711
PheGenIrs199472711
hapmaprs199472711
1000 genomesrs199472711
hgdprs199472711
ensemblrs199472711
gopubmedrs199472711
geneviewrs199472711
scholarrs199472711
googlers199472711
pharmgkbrs199472711
gwascentralrs199472711
openSNPrs199472711
23andMers199472711
23andMe allrs199472711
SNP Nexus

SNPshotrs199472711
SNPdbers199472711
MSV3drs199472711
GWAS Ctlgrs199472711
Max Magnitude0
ClinVar
Risk rs199472711(G;G)
Alt rs199472711(G;G)
Reference rs199472711(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.2593281T>G
CLNSRC ClinVar
CLNACC RCV000057737.2,