Gene | SNP | Alleles | Chromosome | Functional Consequence | MAF databasea | P for HWEb |
---|---|---|---|---|---|---|
PER1 | rs2253820 | A/G | 17:8144851 | splice region variant | 0.44 | 0.954 |
 | rs2585405 | C/G | 17:8143454 | missense variant | 0.23 | 0.441 |
PER2 | rs56386336 | A/G | 2:238245307 | 3'prime UTR variant | 0.09 | 1.000 |
 | rs934945 | A/G | 2:238246412 | missense variant | 0.17 | 0.026 |
CRY1 | rs1056560 | G/T | 12:106991832 | 3'prime UTR variant | 0.47 | 0.402 |
 | rs3809236 | C/T | 12:107093269 | 5'prime UTR variant | 0.20 | 0.892 |
CRY2 | rs2292910 | C/A | 11:45882062 | 3'prime UTR variant | 0.42 | 0.994 |
 | rs6798 | C/T | 11:45882926 | 3'prime UTR variant | 0.24 | 0.892 |
BDNF | rs11030099 | A/C | 11:27656036 | 3'prime UTR variant | 0.23 | 0.205 |
 | rs7124442 | C/T | 11:27655494 | 3'prime UTR variant | 0.33 | 0.654 |
 | rs6265 | A/G | 11:27658369 | missense variant | 0.20 | 0.264 |
NTF3 | rs1805149 | A/G | 12:5494441 | missense variant | 0.12 | 0.592 |