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rs794728533

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728533(A;A)
Make rs794728533(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2776029
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728533
ebirs794728533
HLIrs794728533
Exacrs794728533
Varsomers794728533
Maprs794728533
PheGenIrs794728533
hapmaprs794728533
1000 genomesrs794728533
hgdprs794728533
ensemblrs794728533
gopubmedrs794728533
geneviewrs794728533
scholarrs794728533
googlers794728533
pharmgkbrs794728533
gwascentralrs794728533
openSNPrs794728533
23andMers794728533
23andMe allrs794728533
SNP Nexus

SNPshotrs794728533
SNPdbers794728533
MSV3drs794728533
GWAS Ctlgrs794728533
Max Magnitude0
ClinVar
Risk rs794728533(A;A)
Alt rs794728533(A;A)
Reference rs794728533(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2797259G>A
CLNSRC
CLNACC RCV000182210.2,