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rs199472803

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472803(C;C)
Make rs199472803(C;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2776996
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472803
ebirs199472803
HLIrs199472803
Exacrs199472803
Varsomers199472803
Maprs199472803
PheGenIrs199472803
hapmaprs199472803
1000 genomesrs199472803
hgdprs199472803
ensemblrs199472803
gopubmedrs199472803
geneviewrs199472803
scholarrs199472803
googlers199472803
pharmgkbrs199472803
gwascentralrs199472803
openSNPrs199472803
23andMers199472803
23andMe allrs199472803
SNP Nexus

SNPshotrs199472803
SNPdbers199472803
MSV3drs199472803
GWAS Ctlgrs199472803
Max Magnitude0
ClinVar
Risk rs199472803(C;C)
Alt rs199472803(C;C)
Reference rs199472803(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2798226T>C
CLNSRC ClinVar
CLNACC RCV000057617.2,