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rs17570669

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs17570669(A;T)
Make rs17570669(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position110815726
is asnp
is mentioned by
dbSNPrs17570669
ebirs17570669
HLIrs17570669
Exacrs17570669
Varsomers17570669
Maprs17570669
PheGenIrs17570669
hapmaprs17570669
1000 genomesrs17570669
hgdprs17570669
ensemblrs17570669
gopubmedrs17570669
geneviewrs17570669
scholarrs17570669
googlers17570669
pharmgkbrs17570669
gwascentralrs17570669
openSNPrs17570669
23andMers17570669
23andMe allrs17570669
SNP Nexus

SNPshotrs17570669
SNPdbers17570669
MSV3drs17570669
GWAS Ctlgrs17570669
GMAF0.03306
Max Magnitude0
? (A;A) (A;T) (T;T) 28
[PMID 20733104OA-icon.png] Independent Susceptibility Markers for Atrial Fibrillation on Chromosome 4q25


[PMID 21760908OA-icon.png] Association between variants on chromosome 4q25, 16q22 and 1q21 and atrial fibrillation in the Polish population