Have questions? Visit https://www.reddit.com/r/SNPedia

rs199472705

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472705(C;C)
Make rs199472705(C;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2571345
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472705
ebirs199472705
HLIrs199472705
Exacrs199472705
Varsomers199472705
Maprs199472705
PheGenIrs199472705
hapmaprs199472705
1000 genomesrs199472705
hgdprs199472705
ensemblrs199472705
gopubmedrs199472705
geneviewrs199472705
scholarrs199472705
googlers199472705
pharmgkbrs199472705
gwascentralrs199472705
openSNPrs199472705
23andMers199472705
23andMe allrs199472705
SNP Nexus

SNPshotrs199472705
SNPdbers199472705
MSV3drs199472705
GWAS Ctlgrs199472705
Max Magnitude0
ClinVar
Risk rs199472705(C;C)
Alt rs199472705(C;C)
Reference rs199472705(T;T)
Significance Pathogenic
Disease Atrial fibrillation Atrial fibrillation Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Atrial fibrillation Atrial fibrillation, familial, 3 Long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2592575T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000057725.2, RCV000115006.2, RCV000232681.1,