| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1191926239 | 0.807 | 0.200 | 9 | 117704539 | missense variant | C/G | snv | 4.0E-06 | 7 | ||
| rs1764391 | 0.790 | 0.160 | 1 | 34795168 | missense variant | C/G;T | snv | 0.30 | 7 | ||
| rs771676129 | 0.827 | 0.080 | 7 | 80671082 | synonymous variant | C/T | snv | 4.0E-06 | 7 | ||
| rs999947969 | 0.827 | 0.080 | 7 | 80671145 | synonymous variant | C/T | snv | 7 | |||
| rs1064039 | 0.827 | 0.200 | 20 | 23637790 | missense variant | C/G;T | snv | 0.20 | 6 | ||
| rs11571836 | 0.827 | 0.200 | 13 | 32399302 | 3 prime UTR variant | A/G;T | snv | 6 | |||
| rs146052672 | 0.851 | 0.160 | 6 | 34242693 | intron variant | -/C | delins | 5 | |||
| rs1799943 | 0.925 | 0.080 | 13 | 32316435 | 5 prime UTR variant | G/A;C;T | snv | 0.25 | 5 | ||
| rs1805017 | 0.851 | 0.240 | 6 | 46716485 | missense variant | C/A;T | snv | 4.0E-06; 0.31 | 5 | ||
| rs770572030 | 0.827 | 0.160 | 18 | 49581427 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 5 | ||
| rs1187513719 | 0.851 | 0.200 | 10 | 94780595 | missense variant | A/G | snv | 4.0E-06 | 4 | ||
| rs199473244 | 0.851 | 0.120 | 3 | 38557251 | missense variant | C/A | snv | 4 | |||
| rs200034939 | 0.882 | 0.080 | 3 | 38557248 | missense variant | C/A | snv | 3.2E-05 | 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 | |||
| rs1076991 | 0.925 | 0.200 | 14 | 64388323 | 5 prime UTR variant | T/C;G | snv | 0.45; 8.1E-06 | 2 | ||
| rs1226052130 | 0.925 | 0.120 | 17 | 47299308 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
| rs740952 | 0.925 | 0.080 | 7 | 150952515 | synonymous variant | G/A;T | snv | 0.30; 7.2E-05 | 2 | ||
| 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 | |||
| rs200478651 | 1.000 | 0.080 | 13 | 113118414 | splice region variant | C/A;T | snv | 8.4E-06; 2.1E-05 | 1 | ||
| rs2804924 | 1.000 | 0.080 | 6 | 13574110 | upstream gene variant | G/A;C;T | snv | 1 | |||
| rs754889760 | 1.000 | 0.080 | 22 | 50571440 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs760761240 | 1.000 | 0.080 | 17 | 34256290 | missense variant | G/A;C | snv | 6.0E-05 | 1 |