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rs794728523

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728523(A;C)
Make rs794728523(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2585210
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728523
ebirs794728523
HLIrs794728523
Exacrs794728523
Varsomers794728523
Maprs794728523
PheGenIrs794728523
hapmaprs794728523
1000 genomesrs794728523
hgdprs794728523
ensemblrs794728523
gopubmedrs794728523
geneviewrs794728523
scholarrs794728523
googlers794728523
pharmgkbrs794728523
gwascentralrs794728523
openSNPrs794728523
23andMers794728523
23andMe allrs794728523
SNP Nexus

SNPshotrs794728523
SNPdbers794728523
MSV3drs794728523
GWAS Ctlgrs794728523
Max Magnitude0
ClinVar
Risk rs794728523(C,G;C,G)
Alt rs794728523(C,G;C,G)
Reference rs794728523(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2606440A>C; NC_000011.9:g.2606440A>G
CLNSRC
CLNACC RCV000182162.2, RCV000182163.2,