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rs397508116

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508116(-;-)
Make rs397508116(-;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2570712
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508116
ebirs397508116
HLIrs397508116
Exacrs397508116
Varsomers397508116
Maprs397508116
PheGenIrs397508116
hapmaprs397508116
1000 genomesrs397508116
hgdprs397508116
ensemblrs397508116
gopubmedrs397508116
geneviewrs397508116
scholarrs397508116
googlers397508116
pharmgkbrs397508116
gwascentralrs397508116
openSNPrs397508116
23andMers397508116
23andMe allrs397508116
SNP Nexus

SNPshotrs397508116
SNPdbers397508116
MSV3drs397508116
GWAS Ctlgrs397508116
Max Magnitude0
ClinVar
Risk rs397508116(;)
Alt rs397508116(;)
Reference rs397508116(T;T)
Significance Pathogenic
Disease Long QT syndrome 1/2 Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome 1/2, digenic Long QT syndrome, LQT1 subtype
Reversed 0
HGVS NC_000011.9:g.2591942delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000003299.2, RCV000046082.2,