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rs397508090

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs397508090(-;-)
Make rs397508090(-;CT)
ReferenceGRCh38 38.1/141
Chromosome11
Position2662053
GeneKCNQ1, KCNQ1OT1
is asnp
is mentioned by
dbSNPrs397508090
ebirs397508090
HLIrs397508090
Exacrs397508090
Varsomers397508090
Maprs397508090
PheGenIrs397508090
hapmaprs397508090
1000 genomesrs397508090
hgdprs397508090
ensemblrs397508090
gopubmedrs397508090
geneviewrs397508090
scholarrs397508090
googlers397508090
pharmgkbrs397508090
gwascentralrs397508090
openSNPrs397508090
23andMers397508090
23andMe allrs397508090
SNP Nexus

SNPshotrs397508090
SNPdbers397508090
MSV3drs397508090
GWAS Ctlgrs397508090
Max Magnitude0
ClinVar
Risk rs397508090(;)
Alt rs397508090(;)
Reference rs397508090(CT;CT)
Significance Untested
Disease Long QT syndrome
Variation info
Gene KCNQ1OT1 KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype
Reversed 0
HGVS NC_000011.9:g.2683283_2683284delCT
CLNSRC ClinVar
CLNACC RCV000045987.2,