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rs794728571

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728571(C;T)
Make rs794728571(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2585260
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728571
ebirs794728571
HLIrs794728571
Exacrs794728571
Varsomers794728571
Maprs794728571
PheGenIrs794728571
hapmaprs794728571
1000 genomesrs794728571
hgdprs794728571
ensemblrs794728571
gopubmedrs794728571
geneviewrs794728571
scholarrs794728571
googlers794728571
pharmgkbrs794728571
gwascentralrs794728571
openSNPrs794728571
23andMers794728571
23andMe allrs794728571
SNP Nexus

SNPshotrs794728571
SNPdbers794728571
MSV3drs794728571
GWAS Ctlgrs794728571
Max Magnitude0
ClinVar
Risk rs794728571(T;T)
Alt rs794728571(T;T)
Reference rs794728571(C;C)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNQ1
CLNDBN Cardiac arrhythmia
Reversed 0
HGVS NC_000011.9:g.2606490C>T
CLNSRC
CLNACC RCV000182314.1,