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rs199473409

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473409(A;C)
Make rs199473409(C;C)
ReferenceGRCh38 38.1/142
Chromosome11
Position2585272
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199473409
ebirs199473409
HLIrs199473409
Exacrs199473409
Varsomers199473409
Maprs199473409
PheGenIrs199473409
hapmaprs199473409
1000 genomesrs199473409
hgdprs199473409
ensemblrs199473409
gopubmedrs199473409
geneviewrs199473409
scholarrs199473409
googlers199473409
pharmgkbrs199473409
gwascentralrs199473409
openSNPrs199473409
23andMers199473409
23andMe allrs199473409
SNP Nexus

SNPshotrs199473409
SNPdbers199473409
MSV3drs199473409
GWAS Ctlgrs199473409
Max Magnitude0
ClinVar
Risk rs199473409(C;C)
Alt rs199473409(C;C)
Reference rs199473409(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2606502A>C
CLNSRC ClinVar
CLNACC RCV000057550.2,