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rs199473471

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473471(C;C)
Make rs199473471(C;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2585212
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199473471
ebirs199473471
HLIrs199473471
Exacrs199473471
Varsomers199473471
Maprs199473471
PheGenIrs199473471
hapmaprs199473471
1000 genomesrs199473471
hgdprs199473471
ensemblrs199473471
gopubmedrs199473471
geneviewrs199473471
scholarrs199473471
googlers199473471
pharmgkbrs199473471
gwascentralrs199473471
openSNPrs199473471
23andMers199473471
23andMe allrs199473471
SNP Nexus

SNPshotrs199473471
SNPdbers199473471
MSV3drs199473471
GWAS Ctlgrs199473471
Max Magnitude0
ClinVar
Risk rs199473471(A,C;A,C)
Alt rs199473471(A,C;A,C)
Reference rs199473471(G;G)
Significance Other
Disease not provided Long QT syndrome Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN not provided Long QT syndrome Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2606442G>A; NC_000011.9:g.2606442G>C
CLNSRC ClinVar
CLNACC RCV000182164.1, RCV000045943.4, RCV000057535.2,