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rs794728553

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728553(A;A)
Make rs794728553(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2445441
GeneKCNQ1, LOC105376521
is asnp
is mentioned by
dbSNPrs794728553
ebirs794728553
HLIrs794728553
Exacrs794728553
Varsomers794728553
Maprs794728553
PheGenIrs794728553
hapmaprs794728553
1000 genomesrs794728553
hgdprs794728553
ensemblrs794728553
gopubmedrs794728553
geneviewrs794728553
scholarrs794728553
googlers794728553
pharmgkbrs794728553
gwascentralrs794728553
openSNPrs794728553
23andMers794728553
23andMe allrs794728553
SNP Nexus

SNPshotrs794728553
SNPdbers794728553
MSV3drs794728553
GWAS Ctlgrs794728553
Max Magnitude0
ClinVar
Risk rs794728553(A;A)
Alt rs794728553(A;A)
Reference rs794728553(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2466671G>A
CLNSRC
CLNACC RCV000182261.2,