rs1799983, NOS3

N. diseases: 246
Disease: Blind Loop Syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Blind Loop Syndrome
CUI: C0005750
Disease: Blind Loop Syndrome
0.010 GeneticVariation BEFREE Association between Glu298Asp/677C-T single nucleotide polymorphism in the eNOS/MTHRF gene and blood stasis syndrome of ischemic stroke. 22940147 2012