Table 2.
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.