| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2824292 | 0.925 | 0.080 | 21 | 17414857 | regulatory region variant | G/A | snv | 0.47 | 3 | ||
| rs974453 | 1.000 | 0.080 | 12 | 20737008 | intron variant | A/G;T | snv | 3 | |||
| rs1049194905 | 0.925 | 0.080 | 3 | 38604063 | synonymous variant | A/G | snv | 2 | |||
| rs12090554 | 0.925 | 0.080 | 1 | 185583216 | intron variant | G/A | snv | 0.15 | 2 | ||
| rs12095080 | 1.000 | 0.080 | 1 | 53911057 | 3 prime UTR variant | A/G | snv | 0.12 | 2 | ||
| rs1237080661 | 0.925 | 0.080 | 3 | 38604780 | stop gained | A/G;T | snv | 2.8E-05 | 2 | ||
| rs13290387 | 0.925 | 0.120 | 9 | 116227647 | intron variant | G/C | snv | 0.54 | 2 | ||
| rs1353342 | 0.925 | 0.080 | 9 | 76259853 | intron variant | A/C | snv | 0.79 | 2 | ||
| rs2227721 | 0.925 | 0.080 | 17 | 28370430 | intron variant | C/A;T | snv | 0.12 | 2 | ||
| rs112443954 | 1.000 | 0.080 | 6 | 13574259 | upstream gene variant | G/C | snv | 0.27 | 1 | ||
| rs1140713 | 1.000 | 0.080 | 9 | 136670833 | intron variant | C/T | snv | 0.13 | 1 | ||
| rs1175571390 | 1.000 | 0.080 | 5 | 53056071 | missense variant | T/C | snv | 1 | |||
| rs1183027238 | 1.000 | 0.080 | 13 | 113118480 | synonymous variant | C/T | snv | 1 | |||
| rs1217035505 | 1.000 | 0.080 | 12 | 121184674 | missense variant | G/A | snv | 1 | |||
| rs1416421760 | 1.000 | 0.080 | 18 | 22168362 | non coding transcript exon variant | C/A | snv | 1.4E-05 | 1 | ||
| rs1445501474 | 1.000 | 0.080 | 18 | 22168521 | intron variant | G/T | snv | 1.4E-05 | 1 | ||
| rs2804924 | 1.000 | 0.080 | 6 | 13574110 | upstream gene variant | G/A;C;T | snv | 1 | |||
| rs9978223 | 1.000 | 0.080 | 21 | 33398052 | upstream gene variant | G/A | snv | 0.24 | 1 | ||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs28940579 | 0.732 | 0.440 | 16 | 3243310 | missense variant | A/G;T | snv | 2.2E-03; 4.0E-06 | 13 | ||
| rs767830104 | 0.752 | 0.280 | 2 | 136115399 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 13 | ||
| rs1267969615 | 0.532 | 0.760 | 17 | 63490960 | missense variant | T/C | snv | 4.0E-06 | 100 | ||
| rs770572030 | 0.827 | 0.160 | 18 | 49581427 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 5 | ||
| rs1255283120 | 0.807 | 0.160 | 1 | 11792345 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 7 | |
| rs751377893 | 0.574 | 0.680 | 1 | 169546513 | missense variant | T/C | snv | 4.0E-06 | 65 |