Have questions? Visit https://www.reddit.com/r/SNPedia

rs199473402

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473402(C;C)
Make rs199473402(C;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2585231
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199473402
ebirs199473402
HLIrs199473402
Exacrs199473402
Varsomers199473402
Maprs199473402
PheGenIrs199473402
hapmaprs199473402
1000 genomesrs199473402
hgdprs199473402
ensemblrs199473402
gopubmedrs199473402
geneviewrs199473402
scholarrs199473402
googlers199473402
pharmgkbrs199473402
gwascentralrs199473402
openSNPrs199473402
23andMers199473402
23andMe allrs199473402
SNP Nexus

SNPshotrs199473402
SNPdbers199473402
MSV3drs199473402
GWAS Ctlgrs199473402
Max Magnitude0
ClinVar
Risk rs199473402(C;C)
Alt rs199473402(C;C)
Reference rs199473402(T;T)
Significance Pathogenic
Disease Long QT syndrome Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2606461T>C
CLNSRC ClinVar
CLNACC RCV000045948.2, RCV000057541.2,