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rs397508087

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508087(-;-)
Make rs397508087(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position2588804
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508087
ebirs397508087
HLIrs397508087
Exacrs397508087
Varsomers397508087
Maprs397508087
PheGenIrs397508087
hapmaprs397508087
1000 genomesrs397508087
hgdprs397508087
ensemblrs397508087
gopubmedrs397508087
geneviewrs397508087
scholarrs397508087
googlers397508087
pharmgkbrs397508087
gwascentralrs397508087
openSNPrs397508087
23andMers397508087
23andMe allrs397508087
SNP Nexus

SNPshotrs397508087
SNPdbers397508087
MSV3drs397508087
GWAS Ctlgrs397508087
Max Magnitude0
ClinVar
Risk rs397508087(;)
Alt rs397508087(;)
Reference rs397508087(C;C)
Significance Pathogenic
Disease Long QT syndrome Cardiac arrhythmia
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype Cardiac arrhythmia
Reversed 0
HGVS NC_000011.9:g.2610034delC
CLNSRC ClinVar
CLNACC RCV000045981.2, RCV000182281.1,