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rs138551008

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs138551008(C;T)
Make rs138551008(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2775977
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs138551008
ebirs138551008
HLIrs138551008
Exacrs138551008
Varsomers138551008
Maprs138551008
PheGenIrs138551008
hapmaprs138551008
1000 genomesrs138551008
hgdprs138551008
ensemblrs138551008
gopubmedrs138551008
geneviewrs138551008
scholarrs138551008
googlers138551008
pharmgkbrs138551008
gwascentralrs138551008
openSNPrs138551008
23andMers138551008
23andMe allrs138551008
SNP Nexus

SNPshotrs138551008
SNPdbers138551008
MSV3drs138551008
GWAS Ctlgrs138551008
Max Magnitude0
ClinVar
Risk rs138551008(A,T;A,T)
Alt rs138551008(A,T;A,T)
Reference rs138551008(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.2797207C>A
CLNSRC ClinVar
CLNACC RCV000046004.2, RCV000182320.2,