Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1188383936
rs1188383936
F2
0.050 GeneticVariation BEFREE MTHFR C677T and FVL G1691A polymorphisms may be risk factors for increased vascular complications in patient with SCD. 23992124

2013
dbSNP: rs1188383936
rs1188383936
F2
0.050 GeneticVariation BEFREE MTHFR polymorphic variant C677T is associated to vascular complications in sickle-cell disease. 22924497

2012
dbSNP: rs1188383936
rs1188383936
F2
0.050 GeneticVariation BEFREE In conclusion, MTHFR C677T polymorphism might be a risk factor for vascular complications in SCD. 16906320

2006
dbSNP: rs1188383936
rs1188383936
F2
0.050 GeneticVariation BEFREE Factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations among patients with sickle cell disease in Eastern Saudi Arabia. 15224376

2004
dbSNP: rs1188383936
rs1188383936
F2
0.050 GeneticVariation BEFREE The prevalence of the prothrombin gene variant (allele 20.210 A), factor V Leiden mutation, and homozygosity for transition 677C-->T in the methylenetetrahydrofolate reductase (MTHFR) gene was determined among patients with sickle cell disease (SCD). 9723576

1998