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rs794728509

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728509(A;C)
Make rs794728509(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2570737
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728509
ebirs794728509
HLIrs794728509
Exacrs794728509
Varsomers794728509
Maprs794728509
PheGenIrs794728509
hapmaprs794728509
1000 genomesrs794728509
hgdprs794728509
ensemblrs794728509
gopubmedrs794728509
geneviewrs794728509
scholarrs794728509
googlers794728509
pharmgkbrs794728509
gwascentralrs794728509
openSNPrs794728509
23andMers794728509
23andMe allrs794728509
SNP Nexus

SNPshotrs794728509
SNPdbers794728509
MSV3drs794728509
GWAS Ctlgrs794728509
Max Magnitude0
ClinVar
Risk rs794728509(C;C)
Alt rs794728509(C;C)
Reference rs794728509(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene KCNQ1
CLNDBN not specified
Reversed 0
HGVS NC_000011.9:g.2591967A>C
CLNSRC
CLNACC RCV000182088.2,