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rs397508119

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508119(C;C)
Make rs397508119(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2570727
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508119
ebirs397508119
HLIrs397508119
Exacrs397508119
Varsomers397508119
Maprs397508119
PheGenIrs397508119
hapmaprs397508119
1000 genomesrs397508119
hgdprs397508119
ensemblrs397508119
gopubmedrs397508119
geneviewrs397508119
scholarrs397508119
googlers397508119
pharmgkbrs397508119
gwascentralrs397508119
openSNPrs397508119
23andMers397508119
23andMe allrs397508119
SNP Nexus

SNPshotrs397508119
SNPdbers397508119
MSV3drs397508119
GWAS Ctlgrs397508119
Max Magnitude0
ClinVar
Risk rs397508119(C;C)
Alt rs397508119(C;C)
Reference rs397508119(T;T)
Significance Untested
Disease Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype
Reversed 0
HGVS NC_000011.9:g.2591957T>C
CLNSRC ClinVar
CLNACC RCV000046093.2,