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rs199472809

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472809(C;T)
Make rs199472809(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2777012
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472809
ebirs199472809
HLIrs199472809
Exacrs199472809
Varsomers199472809
Maprs199472809
PheGenIrs199472809
hapmaprs199472809
1000 genomesrs199472809
hgdprs199472809
ensemblrs199472809
gopubmedrs199472809
geneviewrs199472809
scholarrs199472809
googlers199472809
pharmgkbrs199472809
gwascentralrs199472809
openSNPrs199472809
23andMers199472809
23andMe allrs199472809
SNP Nexus

SNPshotrs199472809
SNPdbers199472809
MSV3drs199472809
GWAS Ctlgrs199472809
Max Magnitude0
ClinVar
Risk rs199472809(T;T)
Alt rs199472809(T;T)
Reference rs199472809(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.2798242C>T
CLNSRC ClinVar
CLNACC RCV000057626.2,