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rs794728528

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728528(C;C)
Make rs794728528(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2587694
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728528
dbSNP (old)rs794728528
ClinGenrs794728528
ebirs794728528
HLIrs794728528
Exacrs794728528
Gnomadrs794728528
Varsomers794728528
Maprs794728528
PheGenIrs794728528
Biobankrs794728528
1000 genomesrs794728528
hgdprs794728528
ensemblrs794728528
gopubmedrs794728528
geneviewrs794728528
scholarrs794728528
googlers794728528
pharmgkbrs794728528
gwascentralrs794728528
openSNPrs794728528
23andMers794728528
23andMe allrs794728528
SNP Nexus

SNPshotrs794728528
SNPdbers794728528
MSV3drs794728528
GWAS Ctlgrs794728528
Max Magnitude0
ClinVar
Risk rs794728528(C;C)
Alt rs794728528(C;C)
Reference Rs794728528(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2608924T>C
CLNSRC
CLNACC RCV000182182.2,