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rs794728524

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728524(G;T)
Make rs794728524(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2585228
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728524
ebirs794728524
HLIrs794728524
Exacrs794728524
Varsomers794728524
Maprs794728524
PheGenIrs794728524
hapmaprs794728524
1000 genomesrs794728524
hgdprs794728524
ensemblrs794728524
gopubmedrs794728524
geneviewrs794728524
scholarrs794728524
googlers794728524
pharmgkbrs794728524
gwascentralrs794728524
openSNPrs794728524
23andMers794728524
23andMe allrs794728524
SNP Nexus

SNPshotrs794728524
SNPdbers794728524
MSV3drs794728524
GWAS Ctlgrs794728524
Max Magnitude0
ClinVar
Risk rs794728524(T;T)
Alt rs794728524(T;T)
Reference rs794728524(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2606458G>T
CLNSRC
CLNACC RCV000182165.2,