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rs199473460

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473460(C;C)
Make rs199473460(C;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2572862
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199473460
ebirs199473460
HLIrs199473460
Exacrs199473460
Varsomers199473460
Maprs199473460
PheGenIrs199473460
hapmaprs199473460
1000 genomesrs199473460
hgdprs199473460
ensemblrs199473460
gopubmedrs199473460
geneviewrs199473460
scholarrs199473460
googlers199473460
pharmgkbrs199473460
gwascentralrs199473460
openSNPrs199473460
23andMers199473460
23andMe allrs199473460
SNP Nexus

SNPshotrs199473460
SNPdbers199473460
MSV3drs199473460
GWAS Ctlgrs199473460
Max Magnitude0
ClinVar
Risk rs199473460(C;C)
Alt rs199473460(C;C)
Reference rs199473460(T;T)
Significance Other
Disease Long QT syndrome Congenital long QT syndrome not provided
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome Congenital long QT syndrome not provided
Reversed 0
HGVS NC_000011.9:g.2594092T>C
CLNSRC ClinVar
CLNACC RCV000046131.5, RCV000057763.2, RCV000182116.2,