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rs794728526

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728526(A;T)
Make rs794728526(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2585302
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728526
ebirs794728526
HLIrs794728526
Exacrs794728526
Varsomers794728526
Maprs794728526
PheGenIrs794728526
hapmaprs794728526
1000 genomesrs794728526
hgdprs794728526
ensemblrs794728526
gopubmedrs794728526
geneviewrs794728526
scholarrs794728526
googlers794728526
pharmgkbrs794728526
gwascentralrs794728526
openSNPrs794728526
23andMers794728526
23andMe allrs794728526
SNP Nexus

SNPshotrs794728526
SNPdbers794728526
MSV3drs794728526
GWAS Ctlgrs794728526
Max Magnitude0
ClinVar
Risk rs794728526(T;T)
Alt rs794728526(T;T)
Reference rs794728526(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2606532A>T
CLNSRC
CLNACC RCV000182176.2,