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rs397508125

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508125(-;-)
Make rs397508125(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position2572861
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508125
ClinGenrs397508125
ebirs397508125
HLIrs397508125
Exacrs397508125
Varsomers397508125
Maprs397508125
PheGenIrs397508125
hapmaprs397508125
1000 genomesrs397508125
hgdprs397508125
ensemblrs397508125
gopubmedrs397508125
geneviewrs397508125
scholarrs397508125
googlers397508125
pharmgkbrs397508125
gwascentralrs397508125
openSNPrs397508125
23andMers397508125
23andMe allrs397508125
SNP Nexus

SNPshotrs397508125
SNPdbers397508125
MSV3drs397508125
GWAS Ctlgrs397508125
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs397508125(C;C)
Significance Pathogenic
Disease Long QT syndrome not provided
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype not provided
Reversed 0
HGVS NC_000011.9:g.2594091delC
CLNSRC ClinVar
CLNACC RCV000046130.2, RCV000182270.2,