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rs794728566

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728566(-;-)
Make rs794728566(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2527966
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728566
dbSNP (classic)rs794728566
ClinGenrs794728566
ebirs794728566
HLIrs794728566
Exacrs794728566
Gnomadrs794728566
Varsomers794728566
LitVarrs794728566
Maprs794728566
PheGenIrs794728566
Biobankrs794728566
1000 genomesrs794728566
hgdprs794728566
ensemblrs794728566
geneviewrs794728566
scholarrs794728566
googlers794728566
pharmgkbrs794728566
gwascentralrs794728566
openSNPrs794728566
23andMers794728566
SNPshotrs794728566
SNPdbers794728566
MSV3drs794728566
GWAS Ctlgrs794728566
Max Magnitude0
ClinVar
Risk rs794728566(-;-)
Alt rs794728566(-;-)
Reference Rs794728566(T;T)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNQ1
CLNDBN Cardiac arrhythmia
Reversed 0
HGVS NC_000011.9:g.2549196delT
CLNSRC
CLNACC RCV000182293.1,