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rs794728573

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728573(A;G)
Make rs794728573(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2768842
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728573
ebirs794728573
HLIrs794728573
Exacrs794728573
Varsomers794728573
Maprs794728573
PheGenIrs794728573
hapmaprs794728573
1000 genomesrs794728573
hgdprs794728573
ensemblrs794728573
gopubmedrs794728573
geneviewrs794728573
scholarrs794728573
googlers794728573
pharmgkbrs794728573
gwascentralrs794728573
openSNPrs794728573
23andMers794728573
23andMe allrs794728573
SNP Nexus

SNPshotrs794728573
SNPdbers794728573
MSV3drs794728573
GWAS Ctlgrs794728573
Max Magnitude0
ClinVar
Risk rs794728573(G;G)
Alt rs794728573(G;G)
Reference rs794728573(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2790072A>G
CLNSRC
CLNACC RCV000182319.1,