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rs794728535

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728535(G;T)
Make rs794728535(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2776986
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728535
ebirs794728535
HLIrs794728535
Exacrs794728535
Varsomers794728535
Maprs794728535
PheGenIrs794728535
hapmaprs794728535
1000 genomesrs794728535
hgdprs794728535
ensemblrs794728535
gopubmedrs794728535
geneviewrs794728535
scholarrs794728535
googlers794728535
pharmgkbrs794728535
gwascentralrs794728535
openSNPrs794728535
23andMers794728535
23andMe allrs794728535
SNP Nexus

SNPshotrs794728535
SNPdbers794728535
MSV3drs794728535
GWAS Ctlgrs794728535
Max Magnitude0
ClinVar
Risk rs794728535(T;T)
Alt rs794728535(T;T)
Reference rs794728535(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2798216G>T
CLNSRC
CLNACC RCV000182214.1,