Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799983
rs1799983
0.020 GeneticVariation BEFREE Genotype frequencies are similar for both the eNOS G894T and T-786C polymorphisms in NTG and HTG patients. 26807726

2016

dbSNP: rs1799983
rs1799983
0.020 GeneticVariation BEFREE Three hundred Caucasian patients with HTG and 127 with NTG were enrolled in the study and genotyped for G894T (rs1799983) and T-786C (rs2070744) in NOS3 and C242T (rs4673) in CYBA. 22919264

2012