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rs199473405

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473405(A;G)
Make rs199473405(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2585249
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199473405
ebirs199473405
HLIrs199473405
Exacrs199473405
Varsomers199473405
Maprs199473405
PheGenIrs199473405
hapmaprs199473405
1000 genomesrs199473405
hgdprs199473405
ensemblrs199473405
gopubmedrs199473405
geneviewrs199473405
scholarrs199473405
googlers199473405
pharmgkbrs199473405
gwascentralrs199473405
openSNPrs199473405
23andMers199473405
23andMe allrs199473405
SNP Nexus

SNPshotrs199473405
SNPdbers199473405
MSV3drs199473405
GWAS Ctlgrs199473405
Max Magnitude0
ClinVar
Risk rs199473405(G;G)
Alt rs199473405(G;G)
Reference rs199473405(A;A)
Significance Pathogenic
Disease Long QT syndrome Congenital long QT syndrome Cardiac arrhythmia
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype Congenital long QT syndrome Cardiac arrhythmia
Reversed 0
HGVS NC_000011.9:g.2606479A>G
CLNSRC ClinVar
CLNACC RCV000045952.2, RCV000057544.2, RCV000182168.1,