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rs397508092

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs397508092(-;-)
Make rs397508092(-;CA)
ReferenceGRCh38 38.1/141
Chromosome11
Position2662080
GeneKCNQ1, KCNQ1OT1
is asnp
is mentioned by
dbSNPrs397508092
ebirs397508092
HLIrs397508092
Exacrs397508092
Varsomers397508092
Maprs397508092
PheGenIrs397508092
hapmaprs397508092
1000 genomesrs397508092
hgdprs397508092
ensemblrs397508092
gopubmedrs397508092
geneviewrs397508092
scholarrs397508092
googlers397508092
pharmgkbrs397508092
gwascentralrs397508092
openSNPrs397508092
23andMers397508092
23andMe allrs397508092
SNP Nexus

SNPshotrs397508092
SNPdbers397508092
MSV3drs397508092
GWAS Ctlgrs397508092
Max Magnitude0
ClinVar
Risk rs397508092(;)
Alt rs397508092(;)
Reference rs397508092(CA;CA)
Significance Pathogenic
Disease Long QT syndrome not provided
Variation info
Gene KCNQ1OT1 KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype not provided
Reversed 0
HGVS NC_000011.9:g.2683310_2683311delCA
CLNSRC ClinVar
CLNACC RCV000045989.2, RCV000182283.1,