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rs794728567

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728567(A;A)
Make rs794728567(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2583482
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728567
ebirs794728567
HLIrs794728567
Exacrs794728567
Varsomers794728567
Maprs794728567
PheGenIrs794728567
hapmaprs794728567
1000 genomesrs794728567
hgdprs794728567
ensemblrs794728567
gopubmedrs794728567
geneviewrs794728567
scholarrs794728567
googlers794728567
pharmgkbrs794728567
gwascentralrs794728567
openSNPrs794728567
23andMers794728567
23andMe allrs794728567
SNP Nexus

SNPshotrs794728567
SNPdbers794728567
MSV3drs794728567
GWAS Ctlgrs794728567
Max Magnitude0
ClinVar
Risk rs794728567(A;A)
Alt rs794728567(A;A)
Reference rs794728567(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2604712G>A
CLNSRC
CLNACC RCV000182296.1,