Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3774959 | 0.925 | 0.080 | 4 | 102589957 | intron variant | G/A | snv | 0.34 | 1 | ||
rs314277 | 0.925 | 0.080 | 6 | 104959787 | intron variant | A/C;G;T | snv | 3 | |||
rs7679673 | 0.677 | 0.440 | 4 | 105140377 | intron variant | C/A | snv | 0.50 | 2 | ||
rs4574118 | 1.000 | 0.080 | 2 | 106331987 | intergenic variant | C/G | snv | 0.84 | 1 | ||
rs367615 | 1.000 | 0.080 | 5 | 109613236 | intergenic variant | C/G;T | snv | 1 | |||
rs11213809 | 1.000 | 0.080 | 11 | 111265020 | intron variant | A/G | snv | 0.74 | 1 | ||
rs3802842 | 0.695 | 0.280 | 11 | 111300984 | intron variant | C/A | snv | 0.71 | 2 | ||
rs10749971 | 1.000 | 0.080 | 11 | 111318433 | upstream gene variant | A/G | snv | 0.27 | 1 | ||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 24 | ||
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 10 | |
rs7086803 | 0.763 | 0.160 | 10 | 112738717 | intron variant | G/A | snv | 0.20 | 1 | ||
rs11196172 | 0.708 | 0.200 | 10 | 112967084 | intron variant | G/A | snv | 0.13 | 1 | ||
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 8 | |||
rs7904519 | 0.763 | 0.240 | 10 | 113014168 | intron variant | A/G | snv | 0.55 | 2 | ||
rs12255372 | 0.667 | 0.480 | 10 | 113049143 | intron variant | G/A;T | snv | 3 | |||
rs6734238 | 1.000 | 0.080 | 2 | 113083453 | upstream gene variant | A/G | snv | 0.39 | 4 | ||
rs551510 | 1.000 | 0.080 | 12 | 114676231 | intron variant | C/T | snv | 0.49 | 1 | ||
rs59336 | 0.776 | 0.160 | 12 | 114678547 | intron variant | T/A;G | snv | 0.49 | 1 | ||
rs515746 | 1.000 | 0.080 | 12 | 114681192 | intron variant | G/A | snv | 0.49 | 0.48 | 1 | |
rs140355816 | 0.790 | 0.080 | 8 | 116562277 | intergenic variant | C/G | snv | 9.8E-03 | 1 | ||
rs16892766 | 0.716 | 0.240 | 8 | 116618444 | intergenic variant | A/C | snv | 9.3E-02 | 2 | ||
rs11986063 | 1.000 | 0.080 | 8 | 116628076 | regulatory region variant | C/T | snv | 0.12 | 1 | ||
rs6469656 | 0.790 | 0.080 | 8 | 116635549 | regulatory region variant | G/A;C | snv | 1 | |||
rs1665650 | 0.752 | 0.160 | 10 | 116727589 | intron variant | T/C | snv | 0.69 | 1 | ||
rs1870481 | 1.000 | 0.080 | 4 | 117741865 | intergenic variant | C/T | snv | 0.55 | 1 |