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rs199473411

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473411(C;T)
Make rs199473411(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2585275
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199473411
ebirs199473411
HLIrs199473411
Exacrs199473411
Varsomers199473411
Maprs199473411
PheGenIrs199473411
hapmaprs199473411
1000 genomesrs199473411
hgdprs199473411
ensemblrs199473411
gopubmedrs199473411
geneviewrs199473411
scholarrs199473411
googlers199473411
pharmgkbrs199473411
gwascentralrs199473411
openSNPrs199473411
23andMers199473411
23andMe allrs199473411
SNP Nexus

SNPshotrs199473411
SNPdbers199473411
MSV3drs199473411
GWAS Ctlgrs199473411
Max Magnitude0
ClinVar
Risk rs199473411(T;T)
Alt rs199473411(T;T)
Reference rs199473411(C;C)
Significance Pathogenic
Disease Long QT syndrome Congenital long QT syndrome not provided
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome Congenital long QT syndrome not provided
Reversed 0
HGVS NC_000011.9:g.2606505C>T
CLNSRC ClinVar
CLNACC RCV000045959.3, RCV000057551.2, RCV000182173.2,