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rs7164569

From SNPedia

Orientationplus
Stabilizedplus
Make rs7164569(A;A)
Make rs7164569(A;G)
Make rs7164569(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position31501727
GeneOTUD7A
is asnp
is mentioned by
dbSNPrs7164569
dbSNP (classic)rs7164569
ClinGenrs7164569
ebirs7164569
HLIrs7164569
Exacrs7164569
Gnomadrs7164569
Varsomers7164569
LitVarrs7164569
Maprs7164569
PheGenIrs7164569
Biobankrs7164569
1000 genomesrs7164569
hgdprs7164569
ensemblrs7164569
geneviewrs7164569
scholarrs7164569
googlers7164569
pharmgkbrs7164569
gwascentralrs7164569
openSNPrs7164569
23andMers7164569
SNPshotrs7164569
SNPdbers7164569
MSV3drs7164569
GWAS Ctlgrs7164569
GMAF0.3508
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23650146OA-icon.png]
Trait Venous thromboembolism
Title A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
Risk Allele A
P-val 3E-6
Odds Ratio 1.15 [1.09-1.23]