VARIANT: 2147v1
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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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