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rs199473445

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473445(G;T)
Make rs199473445(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2445268
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199473445
ebirs199473445
HLIrs199473445
Exacrs199473445
Varsomers199473445
Maprs199473445
PheGenIrs199473445
hapmaprs199473445
1000 genomesrs199473445
hgdprs199473445
ensemblrs199473445
gopubmedrs199473445
geneviewrs199473445
scholarrs199473445
googlers199473445
pharmgkbrs199473445
gwascentralrs199473445
openSNPrs199473445
23andMers199473445
23andMe allrs199473445
SNP Nexus

SNPshotrs199473445
SNPdbers199473445
MSV3drs199473445
GWAS Ctlgrs199473445
Max Magnitude0
ClinVar
Risk rs199473445(T;T)
Alt rs199473445(T;T)
Reference rs199473445(G;G)
Significance Probable-Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2466498G>T
CLNSRC ClinVar
CLNACC RCV000057625.2,