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rs794728532

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728532(G;T)
Make rs794728532(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2768874
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728532
ebirs794728532
HLIrs794728532
Exacrs794728532
Varsomers794728532
Maprs794728532
PheGenIrs794728532
hapmaprs794728532
1000 genomesrs794728532
hgdprs794728532
ensemblrs794728532
gopubmedrs794728532
geneviewrs794728532
scholarrs794728532
googlers794728532
pharmgkbrs794728532
gwascentralrs794728532
openSNPrs794728532
23andMers794728532
23andMe allrs794728532
SNP Nexus

SNPshotrs794728532
SNPdbers794728532
MSV3drs794728532
GWAS Ctlgrs794728532
Max Magnitude0
ClinVar
Risk rs794728532(T;T)
Alt rs794728532(T;T)
Reference rs794728532(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2790104G>T
CLNSRC
CLNACC RCV000182195.1,