Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1217691063
rs1217691063
CUI: C1527411
Disease: Thrombosis of retinal vein
Thrombosis of retinal vein
0.010 GeneticVariation BEFREE our study suggests that HHcy is a possible risk factor for RVT development, while no association was found between RVT and the C677T MTHFR genotype. 19825913

2010