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rs199472771

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472771(G;T)
Make rs199472771(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2587581
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472771
ebirs199472771
HLIrs199472771
Exacrs199472771
Varsomers199472771
Maprs199472771
PheGenIrs199472771
hapmaprs199472771
1000 genomesrs199472771
hgdprs199472771
ensemblrs199472771
gopubmedrs199472771
geneviewrs199472771
scholarrs199472771
googlers199472771
pharmgkbrs199472771
gwascentralrs199472771
openSNPrs199472771
23andMers199472771
23andMe allrs199472771
SNP Nexus

SNPshotrs199472771
SNPdbers199472771
MSV3drs199472771
GWAS Ctlgrs199472771
Max Magnitude0
ClinVar
Risk rs199472771(T;T)
Alt rs199472771(T;T)
Reference rs199472771(G;G)
Significance Pathogenic
Disease Long QT syndrome Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2608811G>T
CLNSRC ClinVar
CLNACC RCV000045968.3, RCV000057563.2,