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rs397508068

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTT;CTT) 0 common in clinvar
Make rs397508068(-;-)
Make rs397508068(-;CTT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2583530
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508068
dbSNP (old)rs397508068
ClinGenrs397508068
ebirs397508068
HLIrs397508068
Exacrs397508068
Gnomadrs397508068
Varsomers397508068
Maprs397508068
PheGenIrs397508068
Biobankrs397508068
1000 genomesrs397508068
hgdprs397508068
ensemblrs397508068
gopubmedrs397508068
geneviewrs397508068
scholarrs397508068
googlers397508068
pharmgkbrs397508068
gwascentralrs397508068
openSNPrs397508068
23andMers397508068
23andMe allrs397508068
SNP Nexus

SNPshotrs397508068
SNPdbers397508068
MSV3drs397508068
GWAS Ctlgrs397508068
Max Magnitude0
ClinVar
Risk rs397508068(-;-)
Alt rs397508068(-;-)
Reference Rs397508068(CTT;CTT)
Significance Pathogenic
Disease Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2604760_2604762delCTT
CLNSRC
CLNACC RCV000045930.3,