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rs220733

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs220733(C;T)
Make rs220733(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position159897771
is asnp
is mentioned by
dbSNPrs220733
ebirs220733
HLIrs220733
Exacrs220733
Varsomers220733
Maprs220733
PheGenIrs220733
hapmaprs220733
1000 genomesrs220733
hgdprs220733
ensemblrs220733
gopubmedrs220733
geneviewrs220733
scholarrs220733
googlers220733
pharmgkbrs220733
gwascentralrs220733
openSNPrs220733
23andMers220733
23andMe allrs220733
SNP Nexus

SNPshotrs220733
SNPdbers220733
MSV3drs220733
GWAS Ctlgrs220733
GMAF0.01469
Max Magnitude0

[PMID 21793630] Association of rs2200733 at 4q25 with early onset of lone atrial fibrillation in young patients


[PMID 22690879OA-icon.png] Genetic polymorphisms for estimating risk of atrial fibrillation: a literature-based meta-analysis