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rs397508096

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508096(C;G)
Make rs397508096(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position2445251
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508096
ebirs397508096
HLIrs397508096
Exacrs397508096
Varsomers397508096
Maprs397508096
PheGenIrs397508096
hapmaprs397508096
1000 genomesrs397508096
hgdprs397508096
ensemblrs397508096
gopubmedrs397508096
geneviewrs397508096
scholarrs397508096
googlers397508096
pharmgkbrs397508096
gwascentralrs397508096
openSNPrs397508096
23andMers397508096
23andMe allrs397508096
SNP Nexus

SNPshotrs397508096
SNPdbers397508096
MSV3drs397508096
GWAS Ctlgrs397508096
Max Magnitude0
ClinVar
Risk rs397508096(G;G)
Alt rs397508096(G;G)
Reference rs397508096(C;C)
Significance Pathogenic
Disease Long QT syndrome not provided
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype not provided
Reversed 0
HGVS NC_000011.9:g.2466481C>G
CLNSRC ClinVar
CLNACC RCV000045993.2, RCV000182246.2,