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rs397508091

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508091(C;T)
Make rs397508091(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2662080
GeneKCNQ1, KCNQ1OT1
is asnp
is mentioned by
dbSNPrs397508091
ebirs397508091
HLIrs397508091
Exacrs397508091
Varsomers397508091
Maprs397508091
PheGenIrs397508091
hapmaprs397508091
1000 genomesrs397508091
hgdprs397508091
ensemblrs397508091
gopubmedrs397508091
geneviewrs397508091
scholarrs397508091
googlers397508091
pharmgkbrs397508091
gwascentralrs397508091
openSNPrs397508091
23andMers397508091
23andMe allrs397508091
SNP Nexus

SNPshotrs397508091
SNPdbers397508091
MSV3drs397508091
GWAS Ctlgrs397508091
Max Magnitude0
ClinVar
Risk rs397508091(T;T)
Alt rs397508091(T;T)
Reference rs397508091(C;C)
Significance Untested
Disease Long QT syndrome
Variation info
Gene KCNQ1OT1 KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype
Reversed 0
HGVS NC_000011.9:g.2683310C>T
CLNSRC ClinVar
CLNACC RCV000045988.2,