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rs794728530

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728530(G;T)
Make rs794728530(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2768851
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728530
ebirs794728530
HLIrs794728530
Exacrs794728530
Varsomers794728530
Maprs794728530
PheGenIrs794728530
hapmaprs794728530
1000 genomesrs794728530
hgdprs794728530
ensemblrs794728530
gopubmedrs794728530
geneviewrs794728530
scholarrs794728530
googlers794728530
pharmgkbrs794728530
gwascentralrs794728530
openSNPrs794728530
23andMers794728530
23andMe allrs794728530
SNP Nexus

SNPshotrs794728530
SNPdbers794728530
MSV3drs794728530
GWAS Ctlgrs794728530
Max Magnitude0
ClinVar
Risk rs794728530(T;T)
Alt rs794728530(T;T)
Reference rs794728530(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2790081G>T
CLNSRC
CLNACC RCV000182193.1,