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rs397508088

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508088(-;-)
Make rs397508088(-;C)
Make rs397508088(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position2588804
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508088
ebirs397508088
HLIrs397508088
Exacrs397508088
Varsomers397508088
Maprs397508088
PheGenIrs397508088
hapmaprs397508088
1000 genomesrs397508088
hgdprs397508088
ensemblrs397508088
gopubmedrs397508088
geneviewrs397508088
scholarrs397508088
googlers397508088
pharmgkbrs397508088
gwascentralrs397508088
openSNPrs397508088
23andMers397508088
23andMe allrs397508088
SNP Nexus

SNPshotrs397508088
SNPdbers397508088
MSV3drs397508088
GWAS Ctlgrs397508088
Max Magnitude0
ClinVar
Risk rs397508088(C;C)
Alt rs397508088(C;C)
Reference rs397508088(;)
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.2610034dupC
CLNSRC ClinVar
CLNACC RCV000045982.2, RCV000182282.1,