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rs794728522

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728522(C;C)
Make rs794728522(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2583538
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728522
ebirs794728522
HLIrs794728522
Exacrs794728522
Varsomers794728522
Maprs794728522
PheGenIrs794728522
hapmaprs794728522
1000 genomesrs794728522
hgdprs794728522
ensemblrs794728522
gopubmedrs794728522
geneviewrs794728522
scholarrs794728522
googlers794728522
pharmgkbrs794728522
gwascentralrs794728522
openSNPrs794728522
23andMers794728522
23andMe allrs794728522
SNP Nexus

SNPshotrs794728522
SNPdbers794728522
MSV3drs794728522
GWAS Ctlgrs794728522
Max Magnitude0
ClinVar
Risk rs794728522(C;C)
Alt rs794728522(C;C)
Reference rs794728522(T;T)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNQ1
CLNDBN Cardiac arrhythmia
Reversed 0
HGVS NC_000011.9:g.2604768T>C
CLNSRC
CLNACC RCV000182156.1,