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rs794728579

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728579(A;T)
Make rs794728579(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2445475
GeneKCNQ1, LOC105376521
is asnp
is mentioned by
dbSNPrs794728579
ebirs794728579
HLIrs794728579
Exacrs794728579
Varsomers794728579
Maprs794728579
PheGenIrs794728579
hapmaprs794728579
1000 genomesrs794728579
hgdprs794728579
ensemblrs794728579
gopubmedrs794728579
geneviewrs794728579
scholarrs794728579
googlers794728579
pharmgkbrs794728579
gwascentralrs794728579
openSNPrs794728579
23andMers794728579
23andMe allrs794728579
SNP Nexus

SNPshotrs794728579
SNPdbers794728579
MSV3drs794728579
GWAS Ctlgrs794728579
Max Magnitude0
ClinVar
Risk rs794728579(T;T)
Alt rs794728579(T;T)
Reference rs794728579(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2466705A>T
CLNSRC
CLNACC RCV000182329.1,