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rs199472787

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472787(C;T)
Make rs199472787(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2768884
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472787
ebirs199472787
HLIrs199472787
Exacrs199472787
Varsomers199472787
Maprs199472787
PheGenIrs199472787
hapmaprs199472787
1000 genomesrs199472787
hgdprs199472787
ensemblrs199472787
gopubmedrs199472787
geneviewrs199472787
scholarrs199472787
googlers199472787
pharmgkbrs199472787
gwascentralrs199472787
openSNPrs199472787
23andMers199472787
23andMe allrs199472787
SNP Nexus

SNPshotrs199472787
SNPdbers199472787
MSV3drs199472787
GWAS Ctlgrs199472787
Max Magnitude0
ClinVar
Risk rs199472787(T;T)
Alt rs199472787(T;T)
Reference rs199472787(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.2790114C>T
CLNSRC ClinVar
CLNACC RCV000057595.2,