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rs794728538

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728538(A;G)
Make rs794728538(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2778030
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728538
ebirs794728538
HLIrs794728538
Exacrs794728538
Varsomers794728538
Maprs794728538
PheGenIrs794728538
hapmaprs794728538
1000 genomesrs794728538
hgdprs794728538
ensemblrs794728538
gopubmedrs794728538
geneviewrs794728538
scholarrs794728538
googlers794728538
pharmgkbrs794728538
gwascentralrs794728538
openSNPrs794728538
23andMers794728538
23andMe allrs794728538
SNP Nexus

SNPshotrs794728538
SNPdbers794728538
MSV3drs794728538
GWAS Ctlgrs794728538
Max Magnitude0
ClinVar
Risk rs794728538(G;G)
Alt rs794728538(G;G)
Reference rs794728538(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2799260A>G
CLNSRC
CLNACC RCV000182229.1,