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rs794728558

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728558(-;-)
Make rs794728558(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2662013
GeneKCNQ1, KCNQ1OT1
is asnp
is mentioned by
dbSNPrs794728558
ClinGenrs794728558
ebirs794728558
HLIrs794728558
Exacrs794728558
Varsomers794728558
Maprs794728558
PheGenIrs794728558
hapmaprs794728558
1000 genomesrs794728558
hgdprs794728558
ensemblrs794728558
gopubmedrs794728558
geneviewrs794728558
scholarrs794728558
googlers794728558
pharmgkbrs794728558
gwascentralrs794728558
openSNPrs794728558
23andMers794728558
23andMe allrs794728558
SNP Nexus

SNPshotrs794728558
SNPdbers794728558
MSV3drs794728558
GWAS Ctlgrs794728558
Max Magnitude0
ClinVar
Risk rs794728558(-;-)
Alt rs794728558(-;-)
Reference Rs794728558(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1OT1 KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2683243delC
CLNSRC
CLNACC RCV000182275.2,