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rs794728517

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728517(C;T)
Make rs794728517(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2583474
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728517
ebirs794728517
HLIrs794728517
Exacrs794728517
Varsomers794728517
Maprs794728517
PheGenIrs794728517
hapmaprs794728517
1000 genomesrs794728517
hgdprs794728517
ensemblrs794728517
gopubmedrs794728517
geneviewrs794728517
scholarrs794728517
googlers794728517
pharmgkbrs794728517
gwascentralrs794728517
openSNPrs794728517
23andMers794728517
23andMe allrs794728517
SNP Nexus

SNPshotrs794728517
SNPdbers794728517
MSV3drs794728517
GWAS Ctlgrs794728517
Max Magnitude0
ClinVar
Risk rs794728517(T;T)
Alt rs794728517(T;T)
Reference rs794728517(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2604704C>T
CLNSRC
CLNACC RCV000182144.1,