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rs397508072

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508072(C;T)
Make rs397508072(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2585245
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508072
ebirs397508072
HLIrs397508072
Exacrs397508072
Varsomers397508072
Maprs397508072
PheGenIrs397508072
hapmaprs397508072
1000 genomesrs397508072
hgdprs397508072
ensemblrs397508072
gopubmedrs397508072
geneviewrs397508072
scholarrs397508072
googlers397508072
pharmgkbrs397508072
gwascentralrs397508072
openSNPrs397508072
23andMers397508072
23andMe allrs397508072
SNP Nexus

SNPshotrs397508072
SNPdbers397508072
MSV3drs397508072
GWAS Ctlgrs397508072
Max Magnitude0
ClinVar
Risk rs397508072(T;T)
Alt rs397508072(T;T)
Reference rs397508072(C;C)
Significance Pathogenic
Disease Long QT syndrome not provided
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome not provided
Reversed 0
HGVS NC_000011.9:g.2606475C>T
CLNSRC ClinVar
CLNACC RCV000045950.3, RCV000182167.2,