| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1051730 | 0.641 | 0.600 | 15 | 78601997 | synonymous variant | G/A | snv | 0.27 | 0.26 | 7 | |
| rs8034191 | 0.695 | 0.440 | 15 | 78513681 | intron variant | T/C | snv | 0.27 | 5 | ||
| rs31489 | 0.763 | 0.320 | 5 | 1342599 | intron variant | C/A | snv | 0.41 | 4 | ||
| rs7671167 | 0.925 | 0.040 | 4 | 88962828 | intron variant | C/T | snv | 0.53 | 4 | ||
| rs10947233 | 0.925 | 0.160 | 6 | 32156647 | intron variant | G/C;T | snv | 3.4E-02 | 4 | ||
| rs13118928 | 0.925 | 0.040 | 4 | 144565237 | intron variant | A/G | snv | 0.33 | 3 | ||
| rs1980057 | 1.000 | 0.040 | 4 | 144564586 | intron variant | C/T | snv | 0.31 | 3 | ||
| rs8040868 | 0.742 | 0.240 | 15 | 78618839 | synonymous variant | T/C | snv | 0.35 | 0.37 | 3 | |
| rs7221059 | 1.000 | 0.040 | 17 | 76992362 | intergenic variant | C/A | snv | 0.24 | 1 | ||
| rs7698250 | 1.000 | 0.040 | 4 | 24514008 | downstream gene variant | C/T | snv | 2.2E-02 | 1 | ||
| rs10411619 | 1.000 | 0.040 | 19 | 12641611 | upstream gene variant | T/C | snv | 7.0E-02 | 1 | ||
| rs7957346 | 1.000 | 0.040 | 12 | 95866696 | 3 prime UTR variant | C/A | snv | 0.58 | 1 |