F2, coagulation factor II, thrombin, 2147

N. diseases: 490; N. variants: 42
Disease: Tonometry ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5896
rs5896
Entrez Id: 2147
Gene Symbol: F2
F2
CUI: C0040420
Disease:
Tonometry 		C 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify new loci influencing intraocular pressure. 29617998 2018