KEGG   VARIANT: 2147v1
Entry
2147v1                      Variant                                
Name
Prothrombin 20210A
Gene
F2  coagulation factor II, thrombin [KO:K01313]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutation 20210G-A
ClinVar: 13310
dbSNP: rs1799963
Reference
PMID:9531249
  Authors
Doggen CJ, Cats VM, Bertina RM, Rosendaal FR
  Title
Interaction of coagulation defects and cardiovascular risk factors: increased risk of myocardial infarction associated with factor V Leiden or prothrombin 20210A.
  Journal
Circulation 97:1037-41 (1998)
DOI:10.1161/01.CIR.97.11.1037
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