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rs199473461

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473461(C;C)
Make rs199473461(C;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2572894
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199473461
ebirs199473461
HLIrs199473461
Exacrs199473461
Varsomers199473461
Maprs199473461
PheGenIrs199473461
hapmaprs199473461
1000 genomesrs199473461
hgdprs199473461
ensemblrs199473461
gopubmedrs199473461
geneviewrs199473461
scholarrs199473461
googlers199473461
pharmgkbrs199473461
gwascentralrs199473461
openSNPrs199473461
23andMers199473461
23andMe allrs199473461
SNP Nexus

SNPshotrs199473461
SNPdbers199473461
MSV3drs199473461
GWAS Ctlgrs199473461
Max Magnitude0
ClinVar
Risk rs199473461(C;C)
Alt rs199473461(C;C)
Reference rs199473461(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.2594124T>C
CLNSRC ClinVar
CLNACC RCV000057773.2,