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rs199473469

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473469(A;G)
Make rs199473469(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2583444
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199473469
ebirs199473469
HLIrs199473469
Exacrs199473469
Varsomers199473469
Maprs199473469
PheGenIrs199473469
hapmaprs199473469
1000 genomesrs199473469
hgdprs199473469
ensemblrs199473469
gopubmedrs199473469
geneviewrs199473469
scholarrs199473469
googlers199473469
pharmgkbrs199473469
gwascentralrs199473469
openSNPrs199473469
23andMers199473469
23andMe allrs199473469
SNP Nexus

SNPshotrs199473469
SNPdbers199473469
MSV3drs199473469
GWAS Ctlgrs199473469
Max Magnitude0
ClinVar
Risk rs199473469(G;G)
Alt rs199473469(G;G)
Reference rs199473469(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2604674A>G
CLNSRC ClinVar
CLNACC RCV000057806.2,