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rs199472798

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472798(A;G)
Make rs199472798(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2776009
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472798
ebirs199472798
HLIrs199472798
Exacrs199472798
Varsomers199472798
Maprs199472798
PheGenIrs199472798
hapmaprs199472798
1000 genomesrs199472798
hgdprs199472798
ensemblrs199472798
gopubmedrs199472798
geneviewrs199472798
scholarrs199472798
googlers199472798
pharmgkbrs199472798
gwascentralrs199472798
openSNPrs199472798
23andMers199472798
23andMe allrs199472798
SNP Nexus

SNPshotrs199472798
SNPdbers199472798
MSV3drs199472798
GWAS Ctlgrs199472798
Max Magnitude0
ClinVar
Risk rs199472798(G;G)
Alt rs199472798(G;G)
Reference rs199472798(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.2797239A>G
CLNSRC ClinVar
CLNACC RCV000057609.2,