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rs794728552

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728552(G;T)
Make rs794728552(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2445419
GeneKCNQ1, LOC105376521
is asnp
is mentioned by
dbSNPrs794728552
ebirs794728552
HLIrs794728552
Exacrs794728552
Varsomers794728552
Maprs794728552
PheGenIrs794728552
hapmaprs794728552
1000 genomesrs794728552
hgdprs794728552
ensemblrs794728552
gopubmedrs794728552
geneviewrs794728552
scholarrs794728552
googlers794728552
pharmgkbrs794728552
gwascentralrs794728552
openSNPrs794728552
23andMers794728552
23andMe allrs794728552
SNP Nexus

SNPshotrs794728552
SNPdbers794728552
MSV3drs794728552
GWAS Ctlgrs794728552
Max Magnitude0
ClinVar
Risk rs794728552(T;T)
Alt rs794728552(T;T)
Reference rs794728552(G;G)
Significance Probable-Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNQ1
CLNDBN Cardiac arrhythmia
Reversed 0
HGVS NC_000011.9:g.2466649G>T
CLNSRC
CLNACC RCV000182258.1,