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rs878854350

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878854350(A;G)
Make rs878854350(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position2776984
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs878854350
ebirs878854350
HLIrs878854350
Exacrs878854350
Varsomers878854350
Maprs878854350
PheGenIrs878854350
hapmaprs878854350
1000 genomesrs878854350
hgdprs878854350
ensemblrs878854350
gopubmedrs878854350
geneviewrs878854350
scholarrs878854350
googlers878854350
pharmgkbrs878854350
gwascentralrs878854350
openSNPrs878854350
23andMers878854350
23andMe allrs878854350
SNP Nexus

SNPshotrs878854350
SNPdbers878854350
MSV3drs878854350
GWAS Ctlgrs878854350
Max Magnitude0
ClinVar
Risk rs878854350(G;G)
Alt rs878854350(G;G)
Reference rs878854350(A;A)
Significance Pathogenic
Disease Long QT syndrome 1
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome 1
Reversed 0
HGVS NC_000011.9:g.2798214A>G
CLNSRC
CLNACC RCV000234808.1,