Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728514

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728514(C;T)
Make rs794728514(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2572892
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728514
ebirs794728514
HLIrs794728514
Exacrs794728514
Varsomers794728514
Maprs794728514
PheGenIrs794728514
hapmaprs794728514
1000 genomesrs794728514
hgdprs794728514
ensemblrs794728514
gopubmedrs794728514
geneviewrs794728514
scholarrs794728514
googlers794728514
pharmgkbrs794728514
gwascentralrs794728514
openSNPrs794728514
23andMers794728514
23andMe allrs794728514
SNP Nexus

SNPshotrs794728514
SNPdbers794728514
MSV3drs794728514
GWAS Ctlgrs794728514
Max Magnitude0
ClinVar
Risk rs794728514(T;T)
Alt rs794728514(T;T)
Reference rs794728514(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2594122C>T
CLNSRC
CLNACC RCV000182122.2,