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rs199473455

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473455(C;T)
Make rs199473455(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2571332
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199473455
ebirs199473455
HLIrs199473455
Exacrs199473455
Varsomers199473455
Maprs199473455
PheGenIrs199473455
hapmaprs199473455
1000 genomesrs199473455
hgdprs199473455
ensemblrs199473455
gopubmedrs199473455
geneviewrs199473455
scholarrs199473455
googlers199473455
pharmgkbrs199473455
gwascentralrs199473455
openSNPrs199473455
23andMers199473455
23andMe allrs199473455
SNP Nexus

SNPshotrs199473455
SNPdbers199473455
MSV3drs199473455
GWAS Ctlgrs199473455
Max Magnitude0
ClinVar
Risk rs199473455(G,T;G,T)
Alt rs199473455(G,T;G,T)
Reference rs199473455(C;C)
Significance Pathogenic
Disease Long QT syndrome Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2592562C>G
CLNSRC ClinVar
CLNACC RCV000046098.3, RCV000057722.2,