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rs199473484

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473484(A;A)
Make rs199473484(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2847875
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199473484
ebirs199473484
HLIrs199473484
Exacrs199473484
Varsomers199473484
Maprs199473484
PheGenIrs199473484
hapmaprs199473484
1000 genomesrs199473484
hgdprs199473484
ensemblrs199473484
gopubmedrs199473484
geneviewrs199473484
scholarrs199473484
googlers199473484
pharmgkbrs199473484
gwascentralrs199473484
openSNPrs199473484
23andMers199473484
23andMe allrs199473484
SNP Nexus

SNPshotrs199473484
SNPdbers199473484
MSV3drs199473484
GWAS Ctlgrs199473484
Max Magnitude0
ClinVar
Risk rs199473484(A;A)
Alt rs199473484(A;A)
Reference rs199473484(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome not specified
Variation info
Gene KCNQ1-AS1 KCNQ1
CLNDBN Congenital long QT syndrome not specified
Reversed 0
HGVS NC_000011.9:g.2869105G>A
CLNSRC ClinVar
CLNACC RCV000057649.2, RCV000182236.2,