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rs199472822

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472822(C;G)
Make rs199472822(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2847860
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472822
ebirs199472822
HLIrs199472822
Exacrs199472822
Varsomers199472822
Maprs199472822
PheGenIrs199472822
hapmaprs199472822
1000 genomesrs199472822
hgdprs199472822
ensemblrs199472822
gopubmedrs199472822
geneviewrs199472822
scholarrs199472822
googlers199472822
pharmgkbrs199472822
gwascentralrs199472822
openSNPrs199472822
23andMers199472822
23andMe allrs199472822
SNP Nexus

SNPshotrs199472822
SNPdbers199472822
MSV3drs199472822
GWAS Ctlgrs199472822
Max Magnitude0
ClinVar
Risk rs199472822(A,G;A,G)
Alt rs199472822(A,G;A,G)
Reference rs199472822(C;C)
Significance Pathogenic
Disease Long QT syndrome Congenital long QT syndrome
Variation info
Gene KCNQ1-AS1 KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2869090C>G
CLNSRC ClinVar
CLNACC RCV000046037.2, RCV000057648.2,