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

rs397508093

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508093(A;A)
Make rs397508093(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position2662082
GeneKCNQ1, KCNQ1OT1
is asnp
is mentioned by
dbSNPrs397508093
ebirs397508093
HLIrs397508093
Exacrs397508093
Varsomers397508093
Maprs397508093
PheGenIrs397508093
hapmaprs397508093
1000 genomesrs397508093
hgdprs397508093
ensemblrs397508093
gopubmedrs397508093
geneviewrs397508093
scholarrs397508093
googlers397508093
pharmgkbrs397508093
gwascentralrs397508093
openSNPrs397508093
23andMers397508093
23andMe allrs397508093
SNP Nexus

SNPshotrs397508093
SNPdbers397508093
MSV3drs397508093
GWAS Ctlgrs397508093
Max Magnitude0
ClinVar
Risk rs397508093(A;A)
Alt rs397508093(A;A)
Reference rs397508093(G;G)
Significance Untested
Disease Long QT syndrome
Variation info
Gene KCNQ1OT1 KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype
Reversed 0
HGVS NC_000011.9:g.2683312G>A
CLNSRC ClinVar
CLNACC RCV000045990.2,