| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs17851770 | 1.000 | 0.040 | 6 | 52492273 | missense variant | A/C | snv | 6.2E-02 | 6.2E-02 | 1 | |
| rs534797617 | 1.000 | 0.040 | 6 | 52479212 | missense variant | A/C;G | snv | 1.6E-05 | 1 | ||
| rs4906902 | 0.724 | 0.200 | 15 | 26774621 | intron variant | A/G | snv | 0.15 | 14 | ||
| rs12059546 | 0.925 | 0.040 | 1 | 239806797 | intron variant | A/G | snv | 0.30 | 2 | ||
| rs527539103 | 1.000 | 0.040 | 6 | 52479703 | missense variant | A/G | snv | 1 | |||
| rs543160745 | 1.000 | 0.040 | 6 | 52424148 | missense variant | A/G | snv | 4.0E-06; 7.6E-05 | 1 | ||
| rs574948354 | 1.000 | 0.040 | 6 | 52492310 | missense variant | A/G | snv | 8.0E-05 | 1 | ||
| rs767833659 | 1.000 | 0.040 | 6 | 52465042 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
| rs780571007 | 1.000 | 0.040 | 6 | 52454113 | missense variant | A/G | snv | 3.2E-05 | 5.6E-05 | 1 | |
| rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
| rs9349688 | 1.000 | 0.040 | 6 | 53897294 | missense variant | A/G;T | snv | 0.12; 5.2E-05 | 1 | ||
| rs121434579 | 0.925 | 0.040 | 5 | 161895774 | missense variant | C/A | snv | 2 | |||
| rs149055334 | 0.925 | 0.040 | 6 | 52424111 | missense variant | C/A | snv | 1.9E-03 | 7.7E-03 | 2 | |
| rs183899632 | 1.000 | 0.040 | 8 | 67746023 | missense variant | C/A;T | snv | 5.6E-05; 4.0E-05 | 1 | ||
| rs211037 | 0.742 | 0.240 | 5 | 162101274 | synonymous variant | C/T | snv | 0.28 | 0.31 | 14 | |
| rs121918817 | 0.882 | 0.040 | 2 | 166045080 | missense variant | C/T | snv | 1.7E-03 | 1.5E-03 | 3 | |
| rs10496964 | 0.925 | 0.040 | 2 | 144602342 | intergenic variant | C/T | snv | 0.12 | 2 | ||
| rs763616736 | 0.925 | 0.080 | 17 | 50576111 | missense variant | C/T | snv | 2 | |||
| rs149998588 | 1.000 | 0.040 | 6 | 52479759 | stop gained | C/T | snv | 3.2E-05 | 1.4E-05 | 1 | |
| rs200191497 | 1.000 | 0.040 | 6 | 52438562 | missense variant | C/T | snv | 7.2E-05 | 1.4E-05 | 1 | |
| rs2029461 | 1.000 | 0.040 | 6 | 34138013 | intron variant | C/T | snv | 0.43 | 1 | ||
| rs371151471 | 1.000 | 0.040 | 6 | 52465092 | missense variant | C/T | snv | 1.2E-03 | 2.0E-04 | 1 | |
| rs377286138 | 1.000 | 0.040 | 6 | 52479064 | missense variant | C/T | snv | 1.1E-04 | 7.0E-05 | 1 | |
| rs527295360 | 1.000 | 0.040 | 6 | 52465035 | missense variant | C/T | snv | 2.1E-04 | 1.5E-04 | 1 | |
| rs764096785 | 1.000 | 0.040 | 6 | 52438370 | missense variant | C/T | snv | 1.2E-05 | 3.5E-05 | 1 |