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rs4133289

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs4133289(A;A)
Make rs4133289(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position159484147
is asnp
is mentioned by
dbSNPrs4133289
ebirs4133289
HLIrs4133289
Exacrs4133289
Varsomers4133289
Maprs4133289
PheGenIrs4133289
hapmaprs4133289
1000 genomesrs4133289
hgdprs4133289
ensemblrs4133289
gopubmedrs4133289
geneviewrs4133289
scholarrs4133289
googlers4133289
pharmgkbrs4133289
gwascentralrs4133289
openSNPrs4133289
23andMers4133289
23andMe allrs4133289
SNP Nexus

SNPshotrs4133289
SNPdbers4133289
MSV3drs4133289
GWAS Ctlgrs4133289
GMAF0.1129
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 17903294OA-icon.png]
Trait Hemostatic factors and hematological phenotypes
Title Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study
Risk Allele
P-val 1.9999999999999999E-7
Odds Ratio NR NR


GET Evidence
rs4133289
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0859375
summary