Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1864325 | 0.882 | 0.160 | 17 | 45900461 | intron variant | C/T | snv | 0.14 | 5 | ||
rs2046210 | 0.708 | 0.280 | 6 | 151627231 | intergenic variant | G/A | snv | 0.41 | 4 | ||
rs3130340 | 0.851 | 0.200 | 6 | 32276850 | intron variant | T/C | snv | 0.25 | 4 | ||
rs7524102 | 0.882 | 0.160 | 1 | 22371954 | intergenic variant | A/G | snv | 0.21 | 4 | ||
rs12568930 | 1.000 | 0.040 | 1 | 22375738 | intergenic variant | T/C | snv | 0.21 | 3 | ||
rs3018362 | 0.882 | 0.120 | 18 | 62414860 | upstream gene variant | A/G | snv | 0.67 | 3 | ||
rs6959212 | 7 | 38088724 | intergenic variant | T/C;G | snv | 3 | |||||
rs10048146 | 1.000 | 0.040 | 16 | 86677054 | regulatory region variant | A/G | snv | 0.17 | 2 | ||
rs10876432 | 12 | 53338107 | intron variant | G/A | snv | 2 | |||||
rs12407028 | 1 | 68182033 | intron variant | T/A;C | snv | 0.35 | 2 | ||||
rs1366594 | 5 | 89080244 | intron variant | A/C | snv | 0.57 | 2 | ||||
rs1430740 | 1 | 68191827 | intron variant | T/C | snv | 0.58 | 2 | ||||
rs2016266 | 1.000 | 0.080 | 12 | 53334171 | intron variant | G/A;C | snv | 2 | |||
rs2062305 | 1.000 | 0.040 | 13 | 42478744 | intron variant | G/A | snv | 0.46 | 2 | ||
rs2062375 | 1.000 | 0.080 | 8 | 118965553 | intergenic variant | G/C | snv | 0.65 | 2 | ||
rs2062377 | 8 | 118995181 | upstream gene variant | T/A | snv | 0.67 | 2 | ||||
rs227584 | 17 | 44148179 | missense variant | A/C | snv | 0.40 | 0.48 | 2 | |||
rs2504063 | 6 | 151769572 | intron variant | A/G | snv | 0.50 | 2 | ||||
rs4233949 | 2 | 54432570 | regulatory region variant | C/A;G | snv | 2 | |||||
rs4355801 | 0.882 | 0.120 | 8 | 118911634 | regulatory region variant | A/G;T | snv | 2 | |||
rs4424296 | 8 | 119001037 | intron variant | C/T | snv | 0.61 | 2 | ||||
rs4591859 | 1.000 | 0.080 | 6 | 151622504 | downstream gene variant | T/C | snv | 0.51 | 2 | ||
rs4727338 | 7 | 96491363 | intron variant | G/C;T | snv | 2 | |||||
rs4869742 | 6 | 151586613 | intron variant | C/A;G;T | snv | 2 | |||||
rs6426749 | 1.000 | 0.080 | 1 | 22384980 | intergenic variant | G/C | snv | 0.19 | 2 |