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rs199472791

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472791(C;T)
Make rs199472791(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2768903
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472791
ebirs199472791
HLIrs199472791
Exacrs199472791
Varsomers199472791
Maprs199472791
PheGenIrs199472791
hapmaprs199472791
1000 genomesrs199472791
hgdprs199472791
ensemblrs199472791
gopubmedrs199472791
geneviewrs199472791
scholarrs199472791
googlers199472791
pharmgkbrs199472791
gwascentralrs199472791
openSNPrs199472791
23andMers199472791
23andMe allrs199472791
SNP Nexus

SNPshotrs199472791
SNPdbers199472791
MSV3drs199472791
GWAS Ctlgrs199472791
Max Magnitude0
ClinVar
Risk rs199472791(T;T)
Alt rs199472791(T;T)
Reference rs199472791(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2790133C>T
CLNSRC ClinVar
CLNACC RCV000057601.2,