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rs794728578

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728578(G;G)
Make rs794728578(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2445471
GeneKCNQ1, LOC105376521
is asnp
is mentioned by
dbSNPrs794728578
ebirs794728578
HLIrs794728578
Exacrs794728578
Varsomers794728578
Maprs794728578
PheGenIrs794728578
hapmaprs794728578
1000 genomesrs794728578
hgdprs794728578
ensemblrs794728578
gopubmedrs794728578
geneviewrs794728578
scholarrs794728578
googlers794728578
pharmgkbrs794728578
gwascentralrs794728578
openSNPrs794728578
23andMers794728578
23andMe allrs794728578
SNP Nexus

SNPshotrs794728578
SNPdbers794728578
MSV3drs794728578
GWAS Ctlgrs794728578
Max Magnitude0
ClinVar
Risk rs794728578(G;G)
Alt rs794728578(G;G)
Reference rs794728578(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2466701T>G
CLNSRC
CLNACC RCV000182328.1,