Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12726299 | 1.000 | 0.040 | 1 | 115983051 | intron variant | G/A | snv | 0.46 | 1 | ||
rs13166776 | 1.000 | 0.040 | 5 | 25971247 | intron variant | T/C | snv | 0.28 | 1 | ||
rs1344706 | 0.701 | 0.160 | 2 | 184913701 | intron variant | A/C;T | snv | 1 | |||
rs1409313 | 1.000 | 0.040 | 10 | 102431844 | intron variant | T/C | snv | 0.85 | 1 | ||
rs1429793 | 1.000 | 0.040 | 11 | 20904710 | intron variant | G/C;T | snv | 1 | |||
rs1475531 | 1.000 | 0.040 | 20 | 14886776 | intron variant | G/T | snv | 0.62 | 1 | ||
rs155806 | 1.000 | 0.040 | 5 | 140970255 | intron variant | A/G | snv | 8.9E-02 | 1 | ||
rs16919315 | 1.000 | 0.040 | 12 | 125599817 | intron variant | C/A;G;T | snv | 1 | |||
rs16976358 | 0.827 | 0.080 | 18 | 42611606 | intron variant | T/C | snv | 1.0E-02 | 1 | ||
rs17007739 | 1.000 | 0.040 | 4 | 83920097 | intron variant | T/G | snv | 0.38 | 1 | ||
rs17134117 | 1.000 | 0.040 | 7 | 3991432 | intron variant | C/T | snv | 9.1E-02 | 1 | ||
rs1718101 | 1.000 | 0.040 | 7 | 146425696 | intron variant | T/C;G | snv | 1 | |||
rs1879532 | 1.000 | 0.040 | 2 | 211574587 | intron variant | T/A;C;G | snv | 1 | |||
rs1930165 | 1.000 | 0.040 | 10 | 54542170 | intron variant | G/A;C | snv | 1 | |||
rs2056412 | 1.000 | 0.040 | 8 | 138401090 | intron variant | T/C | snv | 0.14 | 1 | ||
rs2150291 | 1.000 | 0.040 | 14 | 63864705 | intron variant | T/C | snv | 0.81 | 1 | ||
rs263025 | 1.000 | 0.040 | 3 | 183809830 | intron variant | T/C | snv | 0.45 | 1 | ||
rs263035 | 1.000 | 0.040 | 3 | 183805869 | intron variant | A/G | snv | 0.44 | 1 | ||
rs2710102 | 0.790 | 0.120 | 7 | 147877298 | intron variant | A/G;T | snv | 1 | |||
rs2836439 | 1.000 | 0.040 | 21 | 38493226 | intron variant | C/T | snv | 0.16 | 1 | ||
rs289932 | 1.000 | 0.040 | 2 | 151149511 | intron variant | C/T | snv | 0.39 | 1 | ||
rs3782000 | 1.000 | 0.040 | 11 | 114202153 | intron variant | C/T | snv | 0.18 | 1 | ||
rs3797817 | 1.000 | 0.040 | 5 | 108948641 | intron variant | A/C;G | snv | 1 | |||
rs3827735 | 1.000 | 0.040 | 1 | 114510087 | intron variant | C/A;T | snv | 1 | |||
rs4141463 | 0.925 | 0.040 | 20 | 14766825 | intron variant | T/C | snv | 0.50 | 1 |