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rs794728512

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728512(C;C)
Make rs794728512(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2572036
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728512
ebirs794728512
HLIrs794728512
Exacrs794728512
Varsomers794728512
Maprs794728512
PheGenIrs794728512
hapmaprs794728512
1000 genomesrs794728512
hgdprs794728512
ensemblrs794728512
gopubmedrs794728512
geneviewrs794728512
scholarrs794728512
googlers794728512
pharmgkbrs794728512
gwascentralrs794728512
openSNPrs794728512
23andMers794728512
23andMe allrs794728512
SNP Nexus

SNPshotrs794728512
SNPdbers794728512
MSV3drs794728512
GWAS Ctlgrs794728512
Max Magnitude0
ClinVar
Risk rs794728512(C,G;C,G)
Alt rs794728512(C,G;C,G)
Reference rs794728512(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2593266T>C; NC_000011.9:g.2593266T>G
CLNSRC
CLNACC RCV000182102.1, RCV000182304.2,