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. 2019 May 3;10:283. doi: 10.3389/fendo.2019.00283

Table 2.

The study selected SNPs according to their previous reports, together with reported associated traits and ethnicities.

SNP ID Gene(s) Chr: BP Associated population Associated trait References
rs7553035 RD3 1: 211691706 European R (25)
rs10004839 LOC105377441 4: 138154812 European R (25)
rs6472155 LOC105375878; LOC105375879 8: 65730207 European R (25)
rs17194885 SRC 20: 36068389 European R (25)
rs2811893 MYSM1 1: 59162148 Taiwanese DR (14)
rs17376456 KIAA0825; LOC105379087 5: 93557702 Taiwanese DR (14)
rs12219125 PLXDC2 10: 20593087 Taiwanese DR (14)
rs4838605 ARHGAP22 10: 49699957 Taiwanese DR (14)
rs4462262 LOC105378313; LOC105378314 10: 59189178 Taiwanese DR (14)
rs2038823 HS6ST3 13: 96951433 Taiwanese DR (14)
rs9362054 LINC01611 6: 85178268 Japanese DR (13)
rs9543976 UCHL3 13: 76136648 Chinese DR (26)
rs646776 CELSR2 1: 109818530 European CAD (15)
rs4977574 CDKN2B-AS1 9: 22098574 European CAD (15)
rs8055236 CDH13 16: 83212398 European(British) CAD (27)
rs10911021 LOC105371642; ZNF648 1: 182081960 European CAD (17)
rs7901695 TCF7L2 10: 114754088 African Americans CAD (16)

BP, Base-pair position; CAD, Coronary artery disease; Chr., Chromosome number; DR, Diabetic retinopathy; R, retinopathy; SNP, Single Nucleotide Polymorphism. Individuals diagnosed with R or CAD but without T2DM.