Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10011007 | 4 | 130143535 | intergenic variant | A/C | snv | 8.3E-02 | 1 | ||||
rs10031823 | 4 | 102203874 | intergenic variant | T/C | snv | 0.68 | 1 | ||||
rs10044158 | 5 | 63666886 | intergenic variant | G/A | snv | 0.55 | 1 | ||||
rs10175405 | 2 | 100703250 | regulatory region variant | G/T | snv | 0.33 | 1 | ||||
rs10185725 | 2 | 154607197 | intergenic variant | C/T | snv | 0.35 | 1 | ||||
rs10211032 | 2 | 116565497 | intergenic variant | G/A | snv | 0.47 | 1 | ||||
rs10247993 | 7 | 127440323 | intergenic variant | C/T | snv | 0.66 | 1 | ||||
rs1028045 | 2 | 100704613 | intergenic variant | G/A | snv | 0.38 | 1 | ||||
rs10493450 | 1 | 68807756 | intron variant | A/T | snv | 0.13 | 1 | ||||
rs10515007 | 17 | 52318179 | intergenic variant | C/T | snv | 0.13 | 1 | ||||
rs10733389 | 9 | 23378222 | intron variant | A/C;G;T | snv | 1 | |||||
rs10736180 | 10 | 105603830 | intergenic variant | G/A | snv | 0.50 | 1 | ||||
rs10757416 | 9 | 23344739 | intron variant | C/T | snv | 0.35 | 1 | ||||
rs1078141 | 8 | 141609293 | intron variant | C/T | snv | 0.27 | 1 | ||||
rs10789907 | 11 | 112689091 | intron variant | A/C | snv | 0.54 | 1 | ||||
rs10804681 | 3 | 141941833 | upstream gene variant | A/T | snv | 0.88 | 1 | ||||
rs10807603 | 6 | 16972744 | regulatory region variant | A/G | snv | 0.56 | 1 | ||||
rs10854884 | 22 | 50663471 | intergenic variant | C/A | snv | 0.41 | 1 | ||||
rs10916805 | 1 | 20492166 | regulatory region variant | G/C | snv | 0.13 | 1 | ||||
rs10930011 | 2 | 161045556 | downstream gene variant | T/A;G | snv | 1 | |||||
rs10950995 | 7 | 24135246 | downstream gene variant | T/C | snv | 0.39 | 1 | ||||
rs10954160 | 7 | 127564011 | intergenic variant | A/G;T | snv | 1 | |||||
rs10965787 | 9 | 23345909 | intron variant | A/G | snv | 0.17 | 1 | ||||
rs10965796 | 9 | 23357495 | intron variant | A/C;T | snv | 1 | |||||
rs10965816 | 9 | 23388825 | intron variant | G/C | snv | 0.26 | 1 |