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rs878854348

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854348(C;C)
Make rs878854348(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position2777975
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs878854348
ebirs878854348
HLIrs878854348
Exacrs878854348
Varsomers878854348
Maprs878854348
PheGenIrs878854348
hapmaprs878854348
1000 genomesrs878854348
hgdprs878854348
ensemblrs878854348
gopubmedrs878854348
geneviewrs878854348
scholarrs878854348
googlers878854348
pharmgkbrs878854348
gwascentralrs878854348
openSNPrs878854348
23andMers878854348
23andMe allrs878854348
SNP Nexus

SNPshotrs878854348
SNPdbers878854348
MSV3drs878854348
GWAS Ctlgrs878854348
Max Magnitude0
ClinVar
Risk rs878854348(C;C)
Alt rs878854348(C;C)
Reference rs878854348(G;G)
Significance Pathogenic
Disease Long QT syndrome 1
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome 1
Reversed 0
HGVS NC_000011.9:g.2799205G>C
CLNSRC
CLNACC RCV000234796.1,