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rs794728575

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728575(A;G)
Make rs794728575(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2777006
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728575
ebirs794728575
HLIrs794728575
Exacrs794728575
Varsomers794728575
Maprs794728575
PheGenIrs794728575
hapmaprs794728575
1000 genomesrs794728575
hgdprs794728575
ensemblrs794728575
gopubmedrs794728575
geneviewrs794728575
scholarrs794728575
googlers794728575
pharmgkbrs794728575
gwascentralrs794728575
openSNPrs794728575
23andMers794728575
23andMe allrs794728575
SNP Nexus

SNPshotrs794728575
SNPdbers794728575
MSV3drs794728575
GWAS Ctlgrs794728575
Max Magnitude0
ClinVar
Risk rs794728575(G;G)
Alt rs794728575(G;G)
Reference rs794728575(A;A)
Significance Probable-Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNQ1
CLNDBN Cardiac arrhythmia
Reversed 0
HGVS NC_000011.9:g.2798236A>G
CLNSRC
CLNACC RCV000182322.1,