| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2230724 | 0.851 | 0.120 | 9 | 5081780 | synonymous variant | G/A | snv | 0.53 | 0.62 | 4 | |
| rs41316003 | 1.000 | 0.040 | 9 | 5126343 | missense variant | G/A;C | snv | 4.4E-03 | 1 | ||
| rs142269166 | 1.000 | 0.040 | 9 | 5126715 | missense variant | A/G | snv | 2.0E-03 | 2.1E-03 | 1 | |
| rs56118985 | 0.882 | 0.080 | 9 | 5044432 | missense variant | G/A;C | snv | 1.8E-03; 4.0E-06 | 3 | ||
| rs150221602 | 1.000 | 0.040 | 9 | 5081828 | missense variant | G/C | snv | 4.2E-04 | 5.4E-04 | 1 | |
| rs182123615 | 0.807 | 0.200 | 9 | 5070058 | splice region variant | T/C | snv | 3.6E-04 | 1.1E-03 | 7 | |
| rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 181 | ||
| rs368927897 | 0.790 | 0.240 | 9 | 5072541 | missense variant | G/A;T | snv | 2.8E-05; 6.4E-05 | 8 | ||
| rs759031245 | 1.000 | 0.040 | 9 | 5022025 | missense variant | G/T | snv | 5.2E-05 | 1 | ||
| rs375678155 | 1.000 | 9 | 5064922 | missense variant | G/A;C;T | snv | 1.7E-05; 1.7E-05; 4.2E-06 | 1 | |||
| rs771912975 | 1.000 | 0.040 | 9 | 5055750 | stop gained | C/A;G;T | snv | 4.0E-06; 1.6E-05 | 1 | ||
| rs774709145 | 9 | 5080657 | missense variant | G/A;C | snv | 1.3E-05 | 1 | ||||
| rs777015472 | 1.000 | 0.040 | 9 | 5066740 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs764634461 | 1.000 | 0.080 | 9 | 5072516 | missense variant | T/G | snv | 1.2E-05 | 2.8E-05 | 1 | |
| rs1319313254 | 9 | 5050807 | missense variant | C/T | snv | 4.0E-06 | 1 | ||||
| rs12343867 | 0.790 | 0.200 | 9 | 5074189 | intron variant | T/C | snv | 0.25 | 9 | ||
| rs12342421 | 0.851 | 0.080 | 9 | 5065750 | intron variant | G/C | snv | 0.23 | 4 | ||
| rs10974944 | 0.882 | 0.160 | 9 | 5070831 | intron variant | C/G | snv | 0.25 | 4 | ||
| rs1057520016 | 0.851 | 0.080 | 9 | 5089726 | missense variant | C/A;T | snv | 4 | |||
| rs10974947 | 0.882 | 0.080 | 9 | 5072846 | intron variant | G/A | snv | 0.23 | 3 | ||
| rs10815148 | 0.882 | 0.080 | 9 | 5057284 | intron variant | T/A | snv | 0.33 | 3 | ||
| rs10815144 | 0.882 | 0.080 | 9 | 5010192 | intron variant | G/A | snv | 0.62 | 3 | ||
| rs12349785 | 0.882 | 0.080 | 9 | 5076613 | intron variant | G/C | snv | 0.23 | 3 | ||
| rs4495487 | 0.925 | 0.080 | 9 | 5072798 | intron variant | T/C | snv | 0.23 | 3 | ||
| rs1339159756 | 0.925 | 0.120 | 9 | 5078395 | missense variant | C/G | snv | 2 |