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rs199473463

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473463(C;G)
Make rs199473463(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2572913
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199473463
ebirs199473463
HLIrs199473463
Exacrs199473463
Varsomers199473463
Maprs199473463
PheGenIrs199473463
hapmaprs199473463
1000 genomesrs199473463
hgdprs199473463
ensemblrs199473463
gopubmedrs199473463
geneviewrs199473463
scholarrs199473463
googlers199473463
pharmgkbrs199473463
gwascentralrs199473463
openSNPrs199473463
23andMers199473463
23andMe allrs199473463
SNP Nexus

SNPshotrs199473463
SNPdbers199473463
MSV3drs199473463
GWAS Ctlgrs199473463
Max Magnitude0
ClinVar
Risk rs199473463(G;G)
Alt rs199473463(G;G)
Reference rs199473463(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2594143C>G
CLNSRC ClinVar
CLNACC RCV000057780.2,