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rs1866389

From SNPedia

Orientationminus
Stabilizedminus
Make rs1866389(C;C)
Make rs1866389(C;G)
Make rs1866389(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position80065442
GeneTHBS4
is asnp
is mentioned by
dbSNPrs1866389
ebirs1866389
HLIrs1866389
Exacrs1866389
Varsomers1866389
Maprs1866389
PheGenIrs1866389
hapmaprs1866389
1000 genomesrs1866389
hgdprs1866389
ensemblrs1866389
gopubmedrs1866389
geneviewrs1866389
scholarrs1866389
googlers1866389
pharmgkbrs1866389
gwascentralrs1866389
openSNPrs1866389
23andMers1866389
23andMe allrs1866389
SNP Nexus

SNPshotrs1866389
SNPdbers1866389
MSV3drs1866389
GWAS Ctlgrs1866389
GMAF0.1359
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 22011848] Thrombospondin-4 polymorphism (A387P) predicts cardiovascular risk in postinfarction patients with high HDL cholesterol and C-reactive protein levels

[PMID 18178577] Polymorphisms in thrombospondin genes and myocardial infarction: a case-control study and a meta-analysis of available evidence.

[PMID 18682748OA-icon.png] Analysis of 17,576 potentially functional SNPs in three case-control studies of myocardial infarction.


GET Evidence
THBS4-A387P
aa_change Ala387Pro
aa_change_short A387P
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.178565
summary