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

rs1152591

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common/normal
Make rs1152591(C;T)
Make rs1152591(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position64214130
GeneSYNE2
is asnp
is mentioned by
dbSNPrs1152591
dbSNP (classic)rs1152591
ClinGenrs1152591
ebirs1152591
HLIrs1152591
Exacrs1152591
Gnomadrs1152591
Varsomers1152591
LitVarrs1152591
Maprs1152591
PheGenIrs1152591
Biobankrs1152591
1000 genomesrs1152591
hgdprs1152591
ensemblrs1152591
geneviewrs1152591
scholarrs1152591
googlers1152591
pharmgkbrs1152591
gwascentralrs1152591
openSNPrs1152591
23andMers1152591
SNPshotrs1152591
SNPdbers1152591
MSV3drs1152591
GWAS Ctlgrs1152591
GMAF0.3287
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 22544366OA-icon.png]
Trait
Title Meta-analysis identifies six new susceptibility loci for atrial fibrillation.
Risk Allele A
P-val 6E-13
Odds Ratio 1.1300 None


[PMID 24922803] YIA4 Genetic Risk Markers for Atrial Fibrillation Influence Allelic Expression of Nearby Candidate Genes


[PMID 25196315] The rs3807989 G/A Polymorphism in CAV1 is Associated with the Risk of Atrial Fibrillation in Chinese Han Populations


[PMID 29624624OA-icon.png] Genetic modulation of atrial fibrillation risk in a Hispanic/Latino cohort.