rs1801131, MTHFR

N. diseases: 93
Disease: Retinopathy of Prematurity ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Retinopathy of Prematurity
CUI: C0035344
Disease: Retinopathy of Prematurity
0.010 GeneticVariation BEFREE To assess Factor V Leiden (FVL) (rs6025), Prothrombin G20210A (rs1799963), MTHFR C677T (rs1801133), and MTHFR A1298C (rs1801131) gene mutations as risk factors in the development of retinopathy of prematurity (ROP). 27018927 2016