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rs199472687

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472687(A;A)
Make rs199472687(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2527962
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472687
ebirs199472687
HLIrs199472687
Exacrs199472687
Varsomers199472687
Maprs199472687
PheGenIrs199472687
hapmaprs199472687
1000 genomesrs199472687
hgdprs199472687
ensemblrs199472687
gopubmedrs199472687
geneviewrs199472687
scholarrs199472687
googlers199472687
pharmgkbrs199472687
gwascentralrs199472687
openSNPrs199472687
23andMers199472687
23andMe allrs199472687
SNP Nexus

SNPshotrs199472687
SNPdbers199472687
MSV3drs199472687
GWAS Ctlgrs199472687
Max Magnitude0
ClinVar
Risk rs199472687(A;A)
Alt rs199472687(A;A)
Reference rs199472687(G;G)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene KCNQ1
CLNDBN Atrial fibrillation
Reversed 0
HGVS NC_000011.9:g.2549192G>A
CLNSRC ClinVar
CLNACC RCV000057674.2,