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rs199473396

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473396(A;G)
Make rs199473396(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2570698
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199473396
ebirs199473396
HLIrs199473396
Exacrs199473396
Varsomers199473396
Maprs199473396
PheGenIrs199473396
hapmaprs199473396
1000 genomesrs199473396
hgdprs199473396
ensemblrs199473396
gopubmedrs199473396
geneviewrs199473396
scholarrs199473396
googlers199473396
pharmgkbrs199473396
gwascentralrs199473396
openSNPrs199473396
23andMers199473396
23andMe allrs199473396
SNP Nexus

SNPshotrs199473396
SNPdbers199473396
MSV3drs199473396
GWAS Ctlgrs199473396
Max Magnitude0
ClinVar
Risk rs199473396(G;G)
Alt rs199473396(G;G)
Reference rs199473396(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.2591928A>G
CLNSRC ClinVar
CLNACC RCV000057696.2,