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rs794728539

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728539(A;A)
Make rs794728539(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2778037
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728539
ebirs794728539
HLIrs794728539
Exacrs794728539
Varsomers794728539
Maprs794728539
PheGenIrs794728539
hapmaprs794728539
1000 genomesrs794728539
hgdprs794728539
ensemblrs794728539
gopubmedrs794728539
geneviewrs794728539
scholarrs794728539
googlers794728539
pharmgkbrs794728539
gwascentralrs794728539
openSNPrs794728539
23andMers794728539
23andMe allrs794728539
SNP Nexus

SNPshotrs794728539
SNPdbers794728539
MSV3drs794728539
GWAS Ctlgrs794728539
Max Magnitude0
ClinVar
Risk rs794728539(A;A)
Alt rs794728539(A;A)
Reference rs794728539(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2799267G>A
CLNSRC
CLNACC RCV000182230.1,