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rs199473662

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473662(C;T)
Make rs199473662(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2570718
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199473662
ebirs199473662
HLIrs199473662
Exacrs199473662
Varsomers199473662
Maprs199473662
PheGenIrs199473662
hapmaprs199473662
1000 genomesrs199473662
hgdprs199473662
ensemblrs199473662
gopubmedrs199473662
geneviewrs199473662
scholarrs199473662
googlers199473662
pharmgkbrs199473662
gwascentralrs199473662
openSNPrs199473662
23andMers199473662
23andMe allrs199473662
SNP Nexus

SNPshotrs199473662
SNPdbers199473662
MSV3drs199473662
GWAS Ctlgrs199473662
Max Magnitude0
ClinVar
Risk rs199473662(A,T;A,T)
Alt rs199473662(A,T;A,T)
Reference rs199473662(C;C)
Significance Pathogenic
Disease Long QT syndrome Congenital long QT syndrome not provided
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype Congenital long QT syndrome not provided
Reversed 0
HGVS NC_000011.9:g.2591948C>T
CLNSRC ClinVar
CLNACC RCV000046087.2, RCV000057705.2, RCV000182085.2,