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rs199472808

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472808(A;G)
Make rs199472808(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2777005
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472808
ebirs199472808
HLIrs199472808
Exacrs199472808
Varsomers199472808
Maprs199472808
PheGenIrs199472808
hapmaprs199472808
1000 genomesrs199472808
hgdprs199472808
ensemblrs199472808
gopubmedrs199472808
geneviewrs199472808
scholarrs199472808
googlers199472808
pharmgkbrs199472808
gwascentralrs199472808
openSNPrs199472808
23andMers199472808
23andMe allrs199472808
SNP Nexus

SNPshotrs199472808
SNPdbers199472808
MSV3drs199472808
GWAS Ctlgrs199472808
Max Magnitude0
ClinVar
Risk rs199472808(G;G)
Alt rs199472808(G;G)
Reference rs199472808(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.2798235A>G
CLNSRC ClinVar
CLNACC RCV000057624.2,