dbSNP | Variant location | Gene | Base change | NCBI assembly location (Build GRCh38)a | TaqMan SNP assay ID | Tag SNP (CEU population; HapMap)b | Minor allele frequency (MAF)c | ||||
---|---|---|---|---|---|---|---|---|---|---|---|
GC Patients | Control group | ALL | EUR | CEU | |||||||
rs2273535 | Missense | AURKA | A/T | Chr.20:56386485 | C_25623289_10 | Yes | 0.168 | 0.238 | 0.310 | 0.216 | 0.177 |
rs1047972 | Missense | AURKA | C/T | Chr.20:56386407 | AHX1IRW | No | 0.088 | 0.146 | 0.150 | 0.182 | 0.157 |
rs911160 | Intron | AURKA | G/C | Chr.20:56382507 | C_8947670_10 | Yes | 0.206 | 0.276 | 0.447 | 0.246 | 0.202 |
rs8173 | 3′ UTR | AURKA | G/C | Chr.20:56369735 | C_8947675_10 | No | 0.417 | 0.305 | 0.486 | 0.282 | 0.232 |
rs2241909 | Synonymous | AURKB | A/G | Chr.17:8205021 | C_22272900_10 | No | 0.247 | 0.332 | 0.379 | 0.340 | 0.303 |
rs2289590 | Intron | AURKB | C/A | Chr.17:8207446 | C_15770418_10 | Yes | 0.240 | 0.415 | 0.453 | 0.415 | 0.389 |
rs758099 | Intron | AURKC | C/T | Chr.19:57231966 | C_2581008_1_ | No | 0.284 | 0.302 | 0.375 | 0.255 | 0.253 |
rs11084490 | 5′ UTR | AURKC | C/G | Chr.19:57231104 | C_27847620_10 | Yes | 0.139 | 0.223 | 0.132 | 0.165 | 0.177 |
rs42873 | Intron | PLK1 | G/C | Chr.16:23683411 | C_2392140_10 | Yes | 0.230 | 0.208 | 0.234 | 0.215 | 0.192 |