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rs794728569

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728569(A;G)
Make rs794728569(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2571325
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728569
ebirs794728569
HLIrs794728569
Exacrs794728569
Varsomers794728569
Maprs794728569
PheGenIrs794728569
hapmaprs794728569
1000 genomesrs794728569
hgdprs794728569
ensemblrs794728569
gopubmedrs794728569
geneviewrs794728569
scholarrs794728569
googlers794728569
pharmgkbrs794728569
gwascentralrs794728569
openSNPrs794728569
23andMers794728569
23andMe allrs794728569
SNP Nexus

SNPshotrs794728569
SNPdbers794728569
MSV3drs794728569
GWAS Ctlgrs794728569
Max Magnitude0
ClinVar
Risk rs794728569(G;G)
Alt rs794728569(G;G)
Reference rs794728569(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2592555A>G
CLNSRC
CLNACC RCV000182301.1,