| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs111638916 | 0.925 | 0.080 | X | 108084839 | 3 prime UTR variant | G/A | snv | 3 | |||
| rs12083239 | 0.925 | 0.080 | 1 | 39985357 | intergenic variant | G/A;C | snv | 3 | |||
| rs154268 | 0.925 | 0.080 | 5 | 40795766 | intron variant | C/T | snv | 0.69 | 3 | ||
| rs2172362 | 0.925 | 0.080 | 1 | 39829228 | intergenic variant | T/C | snv | 0.58 | 3 | ||
| rs230310 | 0.925 | 0.080 | 1 | 39842047 | intron variant | A/G;T | snv | 3 | |||
| rs377566281 | 0.925 | 0.080 | 19 | 43552083 | missense variant | C/T | snv | 5.6E-05 | 2.1E-05 | 3 | |
| rs461404 | 0.925 | 0.080 | 5 | 40799438 | upstream gene variant | G/A | snv | 0.70 | 3 | ||
| rs56288038 | 0.925 | 0.080 | 5 | 132483914 | 3 prime UTR variant | G/C | snv | 2.0E-05 | 7.0E-06 | 3 | |
| rs759397296 | 0.925 | 0.080 | 7 | 143294294 | missense variant | T/C | snv | 4.0E-06 | 3 | ||
| rs13420827 | 0.882 | 0.160 | 2 | 25231099 | 3 prime UTR variant | C/G;T | snv | 4 | |||
| rs17664 | 0.882 | 0.120 | 2 | 172504503 | 3 prime UTR variant | A/G;T | snv | 4 | |||
| rs2675 | 0.882 | 0.120 | 3 | 124763266 | 3 prime UTR variant | T/G | snv | 0.17 | 4 | ||
| rs4719839 | 0.882 | 0.120 | 7 | 25946953 | downstream gene variant | G/A;C | snv | 4 | |||
| rs9589207 | 0.925 | 0.080 | 13 | 91351335 | mature miRNA variant | G/A;C | snv | 5.4E-03; 4.0E-06 | 4 | ||
| rs1126772 | 0.851 | 0.320 | 4 | 87983034 | 3 prime UTR variant | A/G | snv | 0.16 | 5 | ||
| rs353639 | 0.851 | 0.120 | 11 | 35162817 | intron variant | T/G | snv | 0.32 | 5 | ||
| rs2269772 | 0.925 | 0.080 | 17 | 50072022 | synonymous variant | C/T | snv | 0.17 | 0.19 | 6 | |
| rs3130 | 0.882 | 0.080 | 4 | 15968315 | 3 prime UTR variant | T/A;C | snv | 6 | |||
| rs41274221 | 0.851 | 0.160 | 7 | 100093577 | mature miRNA variant | C/T | snv | 6.4E-05 | 4.9E-05 | 6 | |
| rs4796030 | 0.827 | 0.120 | 17 | 35003131 | 3 prime UTR variant | A/C | snv | 0.66 | 6 | ||
| rs5273 | 0.827 | 0.080 | 1 | 186674636 | missense variant | A/C;G | snv | 4.0E-06; 7.6E-03 | 1.4E-02 | 6 | |
| rs10074991 | 0.851 | 0.120 | 5 | 40790449 | intron variant | G/A | snv | 0.31 | 7 | ||
| rs13361707 | 0.882 | 0.120 | 5 | 40791782 | intron variant | C/T | snv | 0.31 | 7 | ||
| rs1536309 | 0.851 | 0.160 | 10 | 102435445 | upstream gene variant | A/G | snv | 0.32 | 7 | ||
| rs2808668 | 0.851 | 0.120 | 9 | 97690153 | intron variant | C/G;T | snv | 7 |