Have questions? Visit https://www.reddit.com/r/SNPedia

rs397508133

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508133(A;C)
Make rs397508133(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position2583433
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508133
ebirs397508133
HLIrs397508133
Exacrs397508133
Varsomers397508133
Maprs397508133
PheGenIrs397508133
hapmaprs397508133
1000 genomesrs397508133
hgdprs397508133
ensemblrs397508133
gopubmedrs397508133
geneviewrs397508133
scholarrs397508133
googlers397508133
pharmgkbrs397508133
gwascentralrs397508133
openSNPrs397508133
23andMers397508133
23andMe allrs397508133
SNP Nexus

SNPshotrs397508133
SNPdbers397508133
MSV3drs397508133
GWAS Ctlgrs397508133
Max Magnitude0
ClinVar
Risk rs397508133(C;C)
Alt rs397508133(C;C)
Reference rs397508133(A;A)
Significance Untested
Disease Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype
Reversed 0
HGVS NC_000011.9:g.2604663A>C
CLNSRC ClinVar
CLNACC RCV000046159.2,