Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs495828 | 0.827 | 0.200 | 9 | 133279294 | upstream gene variant | T/G | snv | 0.81 | 18 | ||
rs3764261 | 0.732 | 0.280 | 16 | 56959412 | upstream gene variant | C/A | snv | 0.31 | 17 | ||
rs12229654 | 0.763 | 0.320 | 12 | 110976657 | intergenic variant | T/G | snv | 4.8E-03 | 14 | ||
rs4728142 | 0.732 | 0.320 | 7 | 128933913 | upstream gene variant | G/A | snv | 0.38 | 12 | ||
rs7138803 | 0.827 | 0.240 | 12 | 49853685 | intergenic variant | G/A;T | snv | 12 | |||
rs10938397 | 0.851 | 0.200 | 4 | 45180510 | intergenic variant | A/G | snv | 0.37 | 11 | ||
rs10857147 | 1.000 | 0.040 | 4 | 80259918 | intergenic variant | A/T | snv | 0.25 | 9 | ||
rs1458038 | 0.925 | 0.120 | 4 | 80243569 | intergenic variant | C/T | snv | 0.23 | 9 | ||
rs16998073 | 0.925 | 0.120 | 4 | 80263187 | upstream gene variant | A/G;T | snv | 9 | |||
rs17782313 | 0.683 | 0.480 | 18 | 60183864 | intergenic variant | T/C | snv | 0.24 | 9 | ||
rs11099098 | 0.925 | 0.120 | 4 | 80248758 | intergenic variant | G/C;T | snv | 8 | |||
rs11206510 | 0.763 | 0.240 | 1 | 55030366 | intergenic variant | T/A;C;G | snv | 8 | |||
rs1173771 | 5 | 32814922 | regulatory region variant | A/G | snv | 0.65 | 8 | ||||
rs2943641 | 0.763 | 0.160 | 2 | 226229029 | intergenic variant | T/C | snv | 0.67 | 7 | ||
rs2972146 | 0.882 | 0.040 | 2 | 226235982 | intergenic variant | G/T | snv | 0.72 | 7 | ||
rs13149993 | 4 | 80237391 | regulatory region variant | G/A;C | snv | 6 | |||||
rs1327235 | 20 | 10988382 | intron variant | A/G | snv | 0.46 | 6 | ||||
rs1887320 | 20 | 10985350 | intron variant | G/A | snv | 0.46 | 6 | ||||
rs2643826 | 3 | 27521497 | upstream gene variant | C/T | snv | 0.56 | 6 | ||||
rs35444 | 12 | 115114632 | intergenic variant | A/G | snv | 0.38 | 6 | ||||
rs10184428 | 2 | 164155317 | intron variant | C/A;G | snv | 5 | |||||
rs11953630 | 5 | 158418394 | intergenic variant | C/A;T | snv | 5 | |||||
rs16849225 | 2 | 164050310 | intron variant | C/T | snv | 0.19 | 5 | ||||
rs35443 | 12 | 115115073 | intergenic variant | G/C | snv | 0.40 | 5 | ||||
rs4373814 | 10 | 18131043 | intergenic variant | G/C;T | snv | 5 |