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rs794728518

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728518(A;C)
Make rs794728518(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2583475
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728518
ebirs794728518
HLIrs794728518
Exacrs794728518
Varsomers794728518
Maprs794728518
PheGenIrs794728518
hapmaprs794728518
1000 genomesrs794728518
hgdprs794728518
ensemblrs794728518
gopubmedrs794728518
geneviewrs794728518
scholarrs794728518
googlers794728518
pharmgkbrs794728518
gwascentralrs794728518
openSNPrs794728518
23andMers794728518
23andMe allrs794728518
SNP Nexus

SNPshotrs794728518
SNPdbers794728518
MSV3drs794728518
GWAS Ctlgrs794728518
Max Magnitude0
ClinVar
Risk rs794728518(C;C)
Alt rs794728518(C;C)
Reference rs794728518(A;A)
Significance Pathogenic
Disease not specified
Variation info
Gene KCNQ1
CLNDBN not specified
Reversed 0
HGVS NC_000011.9:g.2604705A>C
CLNSRC
CLNACC RCV000182146.2,