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rs794728576

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728576(C;C)
Make rs794728576(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2778006
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728576
ebirs794728576
HLIrs794728576
Exacrs794728576
Varsomers794728576
Maprs794728576
PheGenIrs794728576
hapmaprs794728576
1000 genomesrs794728576
hgdprs794728576
ensemblrs794728576
gopubmedrs794728576
geneviewrs794728576
scholarrs794728576
googlers794728576
pharmgkbrs794728576
gwascentralrs794728576
openSNPrs794728576
23andMers794728576
23andMe allrs794728576
SNP Nexus

SNPshotrs794728576
SNPdbers794728576
MSV3drs794728576
GWAS Ctlgrs794728576
Max Magnitude0
ClinVar
Risk rs794728576(C;C)
Alt rs794728576(C;C)
Reference rs794728576(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2799236T>C
CLNSRC
CLNACC RCV000182323.1,