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rs794728520

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728520(A;T)
Make rs794728520(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2583522
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728520
ebirs794728520
HLIrs794728520
Exacrs794728520
Varsomers794728520
Maprs794728520
PheGenIrs794728520
hapmaprs794728520
1000 genomesrs794728520
hgdprs794728520
ensemblrs794728520
gopubmedrs794728520
geneviewrs794728520
scholarrs794728520
googlers794728520
pharmgkbrs794728520
gwascentralrs794728520
openSNPrs794728520
23andMers794728520
23andMe allrs794728520
SNP Nexus

SNPshotrs794728520
SNPdbers794728520
MSV3drs794728520
GWAS Ctlgrs794728520
Max Magnitude0
ClinVar
Risk rs794728520(G,T;G,T)
Alt rs794728520(G,T;G,T)
Reference rs794728520(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2604752A>T
CLNSRC
CLNACC RCV000182152.1,