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rs199473663

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473663(G;T)
Make rs199473663(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2585280
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199473663
ebirs199473663
HLIrs199473663
Exacrs199473663
Varsomers199473663
Maprs199473663
PheGenIrs199473663
hapmaprs199473663
1000 genomesrs199473663
hgdprs199473663
ensemblrs199473663
gopubmedrs199473663
geneviewrs199473663
scholarrs199473663
googlers199473663
pharmgkbrs199473663
gwascentralrs199473663
openSNPrs199473663
23andMers199473663
23andMe allrs199473663
SNP Nexus

SNPshotrs199473663
SNPdbers199473663
MSV3drs199473663
GWAS Ctlgrs199473663
Max Magnitude0
ClinVar
Risk rs199473663(T;T)
Alt rs199473663(T;T)
Reference rs199473663(G;G)
Significance Pathogenic
Disease Long QT syndrome Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2606510G>T
CLNSRC ClinVar
CLNACC RCV000045962.2, RCV000057554.2,