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rs199472701

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472701(G;G)
Make rs199472701(G;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2570745
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472701
ebirs199472701
HLIrs199472701
Exacrs199472701
Varsomers199472701
Maprs199472701
PheGenIrs199472701
hapmaprs199472701
1000 genomesrs199472701
hgdprs199472701
ensemblrs199472701
gopubmedrs199472701
geneviewrs199472701
scholarrs199472701
googlers199472701
pharmgkbrs199472701
gwascentralrs199472701
openSNPrs199472701
23andMers199472701
23andMe allrs199472701
SNP Nexus

SNPshotrs199472701
SNPdbers199472701
MSV3drs199472701
GWAS Ctlgrs199472701
Max Magnitude0
ClinVar
Risk rs199472701(G;G)
Alt rs199472701(G;G)
Reference rs199472701(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2591975T>G
CLNSRC ClinVar
CLNACC RCV000057716.2,