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rs794728519

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728519(A;A)
Make rs794728519(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2583487
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728519
ebirs794728519
HLIrs794728519
Exacrs794728519
Varsomers794728519
Maprs794728519
PheGenIrs794728519
hapmaprs794728519
1000 genomesrs794728519
hgdprs794728519
ensemblrs794728519
gopubmedrs794728519
geneviewrs794728519
scholarrs794728519
googlers794728519
pharmgkbrs794728519
gwascentralrs794728519
openSNPrs794728519
23andMers794728519
23andMe allrs794728519
SNP Nexus

SNPshotrs794728519
SNPdbers794728519
MSV3drs794728519
GWAS Ctlgrs794728519
Max Magnitude0
ClinVar
Risk rs794728519(A;A)
Alt rs794728519(A;A)
Reference rs794728519(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2604717G>A
CLNSRC
CLNACC RCV000182151.2,