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rs199472691

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472691(A;T)
Make rs199472691(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2570629
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472691
ebirs199472691
HLIrs199472691
Exacrs199472691
Varsomers199472691
Maprs199472691
PheGenIrs199472691
hapmaprs199472691
1000 genomesrs199472691
hgdprs199472691
ensemblrs199472691
gopubmedrs199472691
geneviewrs199472691
scholarrs199472691
googlers199472691
pharmgkbrs199472691
gwascentralrs199472691
openSNPrs199472691
23andMers199472691
23andMe allrs199472691
SNP Nexus

SNPshotrs199472691
SNPdbers199472691
MSV3drs199472691
GWAS Ctlgrs199472691
Max Magnitude0
ClinVar
Risk rs199472691(T;T)
Alt rs199472691(T;T)
Reference rs199472691(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2591859A>T
CLNSRC ClinVar
CLNACC RCV000057682.2,