rs899127658, F2

N. diseases: 82
Disease: Anemia, Sickle Cell ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
0.020 GeneticVariation BEFREE MTHFR C677T and FVL G1691A polymorphisms may be risk factors for increased vascular complications in patient with SCD. 23992124 2013
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
0.020 GeneticVariation BEFREE We determined if the presence of the factor V gene G1691A mutation (factor V Leiden), the prothrombin gene G20210A variant, and methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism may be risk factors for vascular complications in individuals with SCD. 16906320 2006