Annotation Detail
Information
- Associated Genes
- PTGER2
- Associated Variants
-
NC_000014.9:g.52300623G>A
rs708495
PTGS2 c.*2427C>T ( ENST00000680451.1, ENST00000367468.10 )
PTGS2 c.*2427C>G ( ENST00000680451.1, ENST00000367468.10 )
PTGS2 c.*2427C>A ( ENST00000680451.1, ENST00000367468.10 )
NR_125801.1(PACERR):n.536C>G
NC_000014.9:g.52300623G>A
rs708495
PTGS2 c.*2427C>T ( ENST00000367468.10, ENST00000680451.1 )
PTGS2 c.*2427C>G ( ENST00000367468.10, ENST00000680451.1 )
PTGS2 c.*2427C>A ( ENST00000367468.10, ENST00000680451.1 )
NR_125801.1(PACERR):n.536C>G - Associated Disease
- Cardiovascular Diseases
- Source Database
- DisGeNET
- Description
- We evaluated two PTGS2 (rs20417, rs689470), and three PTGER2 (rs708494/uS5, rs708495/uS7, and chr14: 50 764 013/uS10) gene polymorphisms among 600 Caucasian male participants of the Physicians' Health Study with incident myocardial infarction (MI) or ischemic stroke and 600 age- and smoking-matched controls who remained free of all reported cardiovascular disease.
- Pubmed
- 16879213
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000271441872080303
- Year of publication
- 2006
Drugs