| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs751377893 | 0.574 | 0.680 | 1 | 169546513 | missense variant | T/C | snv | 4.0E-06 | 65 | ||
| rs6025 | 0.637 | 0.560 | 1 | 169549811 | missense variant | C/T | snv | 1.8E-02 | 43 | ||
| rs4950928 | 0.653 | 0.560 | 1 | 203186754 | upstream gene variant | G/A;C;T | snv | 33 | |||
| rs599839 | 0.724 | 0.360 | 1 | 109279544 | downstream gene variant | G/A;C | snv | 27 | |||
| rs646776 | 0.752 | 0.240 | 1 | 109275908 | downstream gene variant | C/T | snv | 0.74 | 25 | ||
| rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 16 | ||
| rs7528419 | 0.851 | 0.080 | 1 | 109274570 | 3 prime UTR variant | A/G | snv | 0.23 | 13 | ||
| rs1194897557 | 0.827 | 0.240 | 1 | 11796276 | missense variant | A/G | snv | 8.0E-06 | 7 | ||
| rs755249 | 1 | 39529402 | 3 prime UTR variant | C/A;T | snv | 5 | |||||
| rs2296172 | 1.000 | 0.080 | 1 | 39370145 | missense variant | A/G;T | snv | 0.19; 8.0E-06 | 4 | ||
| rs6668352 | 1 | 11854772 | downstream gene variant | G/A | snv | 0.24 | 2 | ||||
| rs11206019 | 1 | 52794278 | intron variant | G/T | snv | 0.16 | 1 | ||||
| rs1180341 | 1 | 39527136 | 3 prime UTR variant | T/C | snv | 0.48 | 1 | ||||
| rs235243 | 1 | 12259937 | intron variant | G/T | snv | 0.25 | 1 | ||||
| rs4660214 | 1 | 39265878 | intron variant | T/A;C | snv | 1 | |||||
| rs6698723 | 1 | 88400462 | intron variant | A/G | snv | 0.95 | 1 | ||||
| rs767830104 | 0.752 | 0.280 | 2 | 136115399 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 13 | ||
| rs950880 | 1.000 | 0.040 | 2 | 102316102 | intron variant | C/A | snv | 0.30 | 3 | ||
| rs13389599 | 2 | 76861472 | intron variant | T/C | snv | 2.6E-02 | 1 | ||||
| rs16837982 | 2 | 154682843 | intergenic variant | G/T | snv | 5.5E-02 | 1 | ||||
| rs17019537 | 2 | 36708365 | intron variant | T/C;G | snv | 1 | |||||
| rs634138 | 2 | 160876023 | upstream gene variant | C/T | snv | 2.2E-02 | 1 | ||||
| rs1501299 | 0.597 | 0.720 | 3 | 186853334 | intron variant | G/C;T | snv | 52 | |||
| rs2241766 | 0.608 | 0.720 | 3 | 186853103 | synonymous variant | T/C;G | snv | 8.0E-06; 0.13 | 48 |