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rs794728537

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728537(C;T)
Make rs794728537(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2778023
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728537
ebirs794728537
HLIrs794728537
Exacrs794728537
Varsomers794728537
Maprs794728537
PheGenIrs794728537
hapmaprs794728537
1000 genomesrs794728537
hgdprs794728537
ensemblrs794728537
gopubmedrs794728537
geneviewrs794728537
scholarrs794728537
googlers794728537
pharmgkbrs794728537
gwascentralrs794728537
openSNPrs794728537
23andMers794728537
23andMe allrs794728537
SNP Nexus

SNPshotrs794728537
SNPdbers794728537
MSV3drs794728537
GWAS Ctlgrs794728537
Max Magnitude0
ClinVar
Risk rs794728537(T;T)
Alt rs794728537(T;T)
Reference rs794728537(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2799253C>T
CLNSRC
CLNACC RCV000182227.2,