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rs794728536

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728536(A;T)
Make rs794728536(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2778005
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728536
ebirs794728536
HLIrs794728536
Exacrs794728536
Varsomers794728536
Maprs794728536
PheGenIrs794728536
hapmaprs794728536
1000 genomesrs794728536
hgdprs794728536
ensemblrs794728536
gopubmedrs794728536
geneviewrs794728536
scholarrs794728536
googlers794728536
pharmgkbrs794728536
gwascentralrs794728536
openSNPrs794728536
23andMers794728536
23andMe allrs794728536
SNP Nexus

SNPshotrs794728536
SNPdbers794728536
MSV3drs794728536
GWAS Ctlgrs794728536
Max Magnitude0
ClinVar
Risk rs794728536(T;T)
Alt rs794728536(T;T)
Reference rs794728536(A;A)
Significance Pathogenic
Disease not provided Long QT syndrome 1
Variation info
Gene KCNQ1
CLNDBN not provided Long QT syndrome 1
Reversed 0
HGVS NC_000011.9:g.2799235A>T
CLNSRC Sir Ganga Ram Hospital
CLNACC RCV000182222.1, RCV000234786.1,