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rs794728534

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728534(A;A)
Make rs794728534(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2776051
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728534
ebirs794728534
HLIrs794728534
Exacrs794728534
Varsomers794728534
Maprs794728534
PheGenIrs794728534
hapmaprs794728534
1000 genomesrs794728534
hgdprs794728534
ensemblrs794728534
gopubmedrs794728534
geneviewrs794728534
scholarrs794728534
googlers794728534
pharmgkbrs794728534
gwascentralrs794728534
openSNPrs794728534
23andMers794728534
23andMe allrs794728534
SNP Nexus

SNPshotrs794728534
SNPdbers794728534
MSV3drs794728534
GWAS Ctlgrs794728534
Max Magnitude0
ClinVar
Risk rs794728534(A;A)
Alt rs794728534(A;A)
Reference rs794728534(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2797281G>A
CLNSRC
CLNACC RCV000182213.1,