Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1000972 | 20 | 6641070 | regulatory region variant | T/A;G | snv | 2 | |||||
rs1074765 | 6 | 109360458 | intergenic variant | T/C | snv | 0.52 | 2 | ||||
rs117642368 | 17 | 45321692 | upstream gene variant | G/C | snv | 6.9E-02 | 3 | ||||
rs12198986 | 6 | 7719826 | regulatory region variant | G/A | snv | 0.37 | 4 | ||||
rs1388242 | 6 | 45682278 | TF binding site variant | T/C | snv | 0.35 | 2 | ||||
rs2079795 | 17 | 61419288 | regulatory region variant | T/A;C | snv | 3 | |||||
rs2145272 | 20 | 6645571 | intergenic variant | G/A;T | snv | 8 | |||||
rs34811474 | 1.000 | 0.040 | 4 | 25407216 | missense variant | G/A;T | snv | 0.15; 4.1E-06 | 8 | ||
rs1472565 | 1 | 19428536 | intron variant | T/A;C | snv | 2 | |||||
rs2294214 | 0.882 | 0.040 | 6 | 22056694 | splice region variant | A/C;T | snv | 6 | |||
rs2812208 | 13 | 50132951 | intron variant | G/A;C | snv | 5 | |||||
rs3791679 | 0.925 | 0.120 | 2 | 55869757 | intron variant | A/G | snv | 0.20 | 11 | ||
rs10283100 | 8 | 119583783 | missense variant | A/G;T | snv | 0.96 | 3 | ||||
rs143384 | 0.827 | 0.200 | 20 | 35437976 | 5 prime UTR variant | G/A | snv | 0.44 | 17 | ||
rs17134767 | 6 | 2195682 | intron variant | T/C | snv | 0.31 | 2 | ||||
rs73148102 | 7 | 65973877 | intron variant | G/A | snv | 0.14 | 2 | ||||
rs4252548 | 1.000 | 0.040 | 19 | 55368304 | missense variant | C/T | snv | 2.1E-02 | 1.8E-02 | 4 | |
rs6977416 | 7 | 150845623 | intron variant | G/A | snv | 0.48 | 2 | ||||
rs8067165 | 17 | 8128618 | upstream gene variant | C/A;G;T | snv | 3 | |||||
rs6918725 | 6 | 126669246 | intron variant | T/G | snv | 0.50 | 4 | ||||
rs4337252 | 1.000 | 0.040 | 15 | 73934424 | intron variant | G/C | snv | 0.52 | 4 | ||
rs34093919 | 19 | 40611394 | missense variant | G/A | snv | 7.7E-03 | 7.5E-03 | 3 | |||
rs9435733 | 1 | 16981759 | intron variant | T/C | snv | 0.41 | 3 | ||||
rs187799739 | 1 | 150452900 | intron variant | C/A;G | snv | 2 | |||||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 34 |