Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs39059
rs39059
CHN2
0.020 GeneticVariation BEFREE This case-control study comprised of 171 individuals with DR and 548 without DR. Four rs39059, rs2023908, rs1002630 and rs1362363 polymorphism of CHN2 were genotyped for each subjects. 24854763

2015
dbSNP: rs39059
rs39059
CHN2
0.020 GeneticVariation BEFREE In this study, we found CPVL/CHN2 rs39059 was associated with diabetic retinopathy in the Chinese type 2 diabetic patients. 21911749

2011