| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10132733 | 1.000 | 0.040 | 14 | 22477241 | intron variant | A/G | snv | 0.19 | 1 | ||
| rs10483273 | 1.000 | 0.040 | 14 | 22448054 | intron variant | A/G | snv | 9.5E-02 | 1 | ||
| rs10932572 | 1.000 | 0.040 | 2 | 214762673 | intron variant | A/G | snv | 0.42 | 1 | ||
| rs11623995 | 1.000 | 0.040 | 14 | 22436733 | intron variant | A/G | snv | 0.74 | 1 | ||
| rs11624054 | 1.000 | 0.040 | 14 | 22406085 | intron variant | A/G | snv | 0.71 | 1 | ||
| rs11984094 | 1.000 | 0.040 | 7 | 38323965 | upstream gene variant | A/G | snv | 0.14 | 1 | ||
| rs1374230 | 1.000 | 0.040 | 2 | 214754055 | intron variant | A/G | snv | 0.31 | 1 | ||
| rs1860517 | 1.000 | 0.040 | 7 | 38291209 | downstream gene variant | A/G | snv | 0.53 | 1 | ||
| rs2128997 | 1.000 | 0.040 | 14 | 22492115 | upstream gene variant | A/G | snv | 0.27 | 1 | ||
| rs2141988 | 1.000 | 0.040 | 14 | 22434470 | intron variant | A/G | snv | 0.44 | 1 | ||
| rs2240826 | 1.000 | 0.040 | 7 | 38279738 | upstream gene variant | A/G | snv | 9.9E-02 | 1 | ||
| rs2240839 | 1.000 | 0.040 | 7 | 38302324 | upstream gene variant | A/G | snv | 0.45 | 1 | ||
| rs2240848 | 1.000 | 0.040 | 7 | 38321866 | upstream gene variant | A/G | snv | 5.5E-02 | 1 | ||
| rs2240849 | 1.000 | 0.040 | 7 | 38322471 | non coding transcript exon variant | A/G | snv | 0.12 | 1 | ||
| rs2301201 | 1.000 | 0.040 | 14 | 22418740 | non coding transcript exon variant | A/G | snv | 0.20 | 0.17 | 1 | |
| rs2733776 | 1.000 | 0.040 | 14 | 22461795 | intron variant | A/G | snv | 0.24 | 1 | ||
| rs4982635 | 1.000 | 0.040 | 14 | 22411336 | intron variant | A/G | snv | 0.24 | 1 | ||
| rs7147975 | 1.000 | 0.040 | 14 | 22022482 | intergenic variant | A/G | snv | 0.48 | 1 | ||
| rs7155927 | 1.000 | 0.040 | 14 | 22263097 | intron variant | A/G | snv | 0.23 | 1 | ||
| rs7584646 | 1.000 | 0.040 | 2 | 214764598 | intron variant | A/G | snv | 0.41 | 1 | ||
| rs7782269 | 1.000 | 0.040 | 7 | 38278989 | upstream gene variant | A/G | snv | 0.42 | 1 | ||
| rs8022578 | 1.000 | 0.040 | 14 | 22101908 | upstream gene variant | A/G | snv | 0.30 | 1 | ||
| rs201698323 | 0.851 | 0.120 | 3 | 38742448 | missense variant | A/G;T | snv | 5.9E-04 | 4 | ||
| rs758576072 | 0.851 | 0.160 | 8 | 104244917 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 4 | ||
| rs2240851 | 1.000 | 0.040 | 7 | 38324328 | upstream gene variant | A/G;T | snv | 1 |