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rs199472725

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472725(G;G)
Make rs199472725(G;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2572868
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472725
ebirs199472725
HLIrs199472725
Exacrs199472725
Varsomers199472725
Maprs199472725
PheGenIrs199472725
hapmaprs199472725
1000 genomesrs199472725
hgdprs199472725
ensemblrs199472725
gopubmedrs199472725
geneviewrs199472725
scholarrs199472725
googlers199472725
pharmgkbrs199472725
gwascentralrs199472725
openSNPrs199472725
23andMers199472725
23andMe allrs199472725
SNP Nexus

SNPshotrs199472725
SNPdbers199472725
MSV3drs199472725
GWAS Ctlgrs199472725
Max Magnitude0
ClinVar
Risk rs199472725(G;G)
Alt rs199472725(G;G)
Reference rs199472725(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome not provided
Variation info
Gene KCNQ1
CLNDBN Congenital long QT syndrome not provided
Reversed 0
HGVS NC_000011.9:g.2594098T>G
CLNSRC ClinVar
CLNACC RCV000057764.2, RCV000182117.2,