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rs199472732

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472732(A;G)
Make rs199472732(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2572907
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472732
ebirs199472732
HLIrs199472732
Exacrs199472732
Varsomers199472732
Maprs199472732
PheGenIrs199472732
hapmaprs199472732
1000 genomesrs199472732
hgdprs199472732
ensemblrs199472732
gopubmedrs199472732
geneviewrs199472732
scholarrs199472732
googlers199472732
pharmgkbrs199472732
gwascentralrs199472732
openSNPrs199472732
23andMers199472732
23andMe allrs199472732
SNP Nexus

SNPshotrs199472732
SNPdbers199472732
MSV3drs199472732
GWAS Ctlgrs199472732
Max Magnitude0
ClinVar
Risk rs199472732(G;G)
Alt rs199472732(G;G)
Reference rs199472732(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.2594137A>G
CLNSRC ClinVar
CLNACC RCV000057778.2,