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rs397508089

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508089(-;-)
Make rs397508089(-;G)
Make rs397508089(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position2588806
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508089
ebirs397508089
HLIrs397508089
Exacrs397508089
Varsomers397508089
Maprs397508089
PheGenIrs397508089
hapmaprs397508089
1000 genomesrs397508089
hgdprs397508089
ensemblrs397508089
gopubmedrs397508089
geneviewrs397508089
scholarrs397508089
googlers397508089
pharmgkbrs397508089
gwascentralrs397508089
openSNPrs397508089
23andMers397508089
23andMe allrs397508089
SNP Nexus

SNPshotrs397508089
SNPdbers397508089
MSV3drs397508089
GWAS Ctlgrs397508089
Max Magnitude0
ClinVar
Risk rs397508089(G;G)
Alt rs397508089(G;G)
Reference rs397508089(;)
Significance Untested
Disease Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype
Reversed 0
HGVS NC_000011.9:g.2610036dupG
CLNSRC ClinVar
CLNACC RCV000045983.2,