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rs199473408

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473408(A;A)
Make rs199473408(A;C)
ReferenceGRCh38 38.1/142
Chromosome11
Position2585266
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199473408
ebirs199473408
HLIrs199473408
Exacrs199473408
Varsomers199473408
Maprs199473408
PheGenIrs199473408
hapmaprs199473408
1000 genomesrs199473408
hgdprs199473408
ensemblrs199473408
gopubmedrs199473408
geneviewrs199473408
scholarrs199473408
googlers199473408
pharmgkbrs199473408
gwascentralrs199473408
openSNPrs199473408
23andMers199473408
23andMe allrs199473408
SNP Nexus

SNPshotrs199473408
SNPdbers199473408
MSV3drs199473408
GWAS Ctlgrs199473408
Max Magnitude0
ClinVar
Risk rs199473408(A;A)
Alt rs199473408(A;A)
Reference rs199473408(C;C)
Significance Pathogenic
Disease Long QT syndrome Congenital long QT syndrome not provided
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype Congenital long QT syndrome not provided
Reversed 0
HGVS NC_000011.9:g.2606496C>A
CLNSRC ClinVar
CLNACC RCV000045958.2, RCV000057549.2, RCV000182172.2,