Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10938397 | 0.851 | 0.200 | 4 | 45180510 | intergenic variant | A/G | snv | 0.37 | 19 | ||
rs7138803 | 0.827 | 0.240 | 12 | 49853685 | intergenic variant | G/A;T | snv | 17 | |||
rs2036527 | 0.851 | 0.080 | 15 | 78559273 | regulatory region variant | G/A | snv | 0.29 | 12 | ||
rs6567160 | 1.000 | 0.080 | 18 | 60161902 | upstream gene variant | T/C | snv | 0.21 | 12 | ||
rs543874 | 1.000 | 0.080 | 1 | 177920345 | upstream gene variant | A/G | snv | 0.21 | 11 | ||
rs998584 | 6 | 43790159 | downstream gene variant | C/A | snv | 0.41 | 11 | ||||
rs2001945 | 8 | 125465736 | upstream gene variant | G/A;C;T | snv | 10 | |||||
rs13141641 | 1.000 | 0.040 | 4 | 144585304 | intron variant | T/C | snv | 0.32 | 8 | ||
rs2820443 | 0.882 | 0.120 | 1 | 219580167 | regulatory region variant | T/C | snv | 0.23 | 8 | ||
rs17451107 | 3 | 157079820 | upstream gene variant | T/C | snv | 0.38 | 7 | ||||
rs4105144 | 0.827 | 0.160 | 19 | 40852719 | intron variant | T/C | snv | 7 | |||
rs10132280 | 14 | 25458973 | intergenic variant | C/A | snv | 0.37 | 6 | ||||
rs29941 | 1.000 | 0.080 | 19 | 33818627 | downstream gene variant | A/G | snv | 0.70 | 6 | ||
rs7166081 | 0.925 | 0.080 | 15 | 67199963 | downstream gene variant | G/A | snv | 0.76 | 6 | ||
rs979012 | 1.000 | 0.080 | 20 | 6642727 | intergenic variant | T/C | snv | 0.67 | 6 | ||
rs10804591 | 3 | 129615390 | intergenic variant | C/A | snv | 0.63 | 5 | ||||
rs11205277 | 1.000 | 0.120 | 1 | 149920979 | upstream gene variant | A/C;G;T | snv | 5 | |||
rs11878604 | 19 | 40827379 | intron variant | T/C | snv | 0.14 | 5 | ||||
rs1884897 | 20 | 6632185 | regulatory region variant | A/G;T | snv | 5 | |||||
rs6556301 | 5 | 177100576 | downstream gene variant | G/T | snv | 0.33 | 5 | ||||
rs7536458 | 1 | 118321979 | intergenic variant | T/G | snv | 0.23 | 5 | ||||
rs10245353 | 7 | 25818994 | intergenic variant | C/A | snv | 0.16 | 4 | ||||
rs10842707 | 12 | 26318431 | intron variant | C/G;T | snv | 4 | |||||
rs10919388 | 1 | 170403362 | intergenic variant | A/C | snv | 0.71 | 4 | ||||
rs12286929 | 0.925 | 0.080 | 11 | 115151684 | intergenic variant | A/C;G | snv | 4 |