Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799983
rs1799983
NOS3
CUI: C0005750
Disease: Blind Loop Syndrome
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