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rs794728510

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728510(C;T)
Make rs794728510(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2570739
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728510
ebirs794728510
HLIrs794728510
Exacrs794728510
Varsomers794728510
Maprs794728510
PheGenIrs794728510
hapmaprs794728510
1000 genomesrs794728510
hgdprs794728510
ensemblrs794728510
gopubmedrs794728510
geneviewrs794728510
scholarrs794728510
googlers794728510
pharmgkbrs794728510
gwascentralrs794728510
openSNPrs794728510
23andMers794728510
23andMe allrs794728510
SNP Nexus

SNPshotrs794728510
SNPdbers794728510
MSV3drs794728510
GWAS Ctlgrs794728510
Max Magnitude0
ClinVar
Risk rs794728510(T;T)
Alt rs794728510(T;T)
Reference rs794728510(C;C)
Significance Pathogenic
Disease not specified
Variation info
Gene KCNQ1
CLNDBN not specified
Reversed 0
HGVS NC_000011.9:g.2591969C>T
CLNSRC
CLNACC RCV000182089.2,