F2, coagulation factor II, thrombin, 2147

N. diseases: 490; N. variants: 42
Disease: Nephrotic Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs552953108
rs552953108
Entrez Id: 2147
Gene Symbol: F2
F2
CUI: C0027726
Disease:
Nephrotic Syndrome 		0.010 GeneticVariation BEFREE We evaluated 53 children with NS and 41 paediatric controls for prevalence of the factor V mutation Arg506-->Gln (factor V Leiden), the prothrombin variant (20210G-->A), and homozygosity for Ala677-->Val in the methylenetetrahydrofolate reductase gene (MTHFR). 9835442 1998