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rs199472802

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472802(G;T)
Make rs199472802(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2776054
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472802
ebirs199472802
HLIrs199472802
Exacrs199472802
Varsomers199472802
Maprs199472802
PheGenIrs199472802
hapmaprs199472802
1000 genomesrs199472802
hgdprs199472802
ensemblrs199472802
gopubmedrs199472802
geneviewrs199472802
scholarrs199472802
googlers199472802
pharmgkbrs199472802
gwascentralrs199472802
openSNPrs199472802
23andMers199472802
23andMe allrs199472802
SNP Nexus

SNPshotrs199472802
SNPdbers199472802
MSV3drs199472802
GWAS Ctlgrs199472802
Max Magnitude0
ClinVar
Risk rs199472802(T;T)
Alt rs199472802(T;T)
Reference rs199472802(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2797284G>T
CLNSRC ClinVar
CLNACC RCV000057616.2,