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rs199472810

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472810(A;A)
Make rs199472810(A;C)
ReferenceGRCh38 38.1/142
Chromosome11
Position2777019
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472810
ebirs199472810
HLIrs199472810
Exacrs199472810
Varsomers199472810
Maprs199472810
PheGenIrs199472810
hapmaprs199472810
1000 genomesrs199472810
hgdprs199472810
ensemblrs199472810
gopubmedrs199472810
geneviewrs199472810
scholarrs199472810
googlers199472810
pharmgkbrs199472810
gwascentralrs199472810
openSNPrs199472810
23andMers199472810
23andMe allrs199472810
SNP Nexus

SNPshotrs199472810
SNPdbers199472810
MSV3drs199472810
GWAS Ctlgrs199472810
Max Magnitude0
ClinVar
Risk rs199472810(A;A)
Alt rs199472810(A;A)
Reference rs199472810(C;C)
Significance Pathogenic
Disease Long QT syndrome Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2798249C>A
CLNSRC ClinVar
CLNACC RCV000046021.2, RCV000057627.2,