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rs794728511

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728511(A;C)
Make rs794728511(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2571399
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728511
ebirs794728511
HLIrs794728511
Exacrs794728511
Varsomers794728511
Maprs794728511
PheGenIrs794728511
hapmaprs794728511
1000 genomesrs794728511
hgdprs794728511
ensemblrs794728511
gopubmedrs794728511
geneviewrs794728511
scholarrs794728511
googlers794728511
pharmgkbrs794728511
gwascentralrs794728511
openSNPrs794728511
23andMers794728511
23andMe allrs794728511
SNP Nexus

SNPshotrs794728511
SNPdbers794728511
MSV3drs794728511
GWAS Ctlgrs794728511
Max Magnitude0
ClinVar
Risk rs794728511(C;C)
Alt rs794728511(C;C)
Reference rs794728511(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2592629A>C
CLNSRC
CLNACC RCV000182097.1,