Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2001945 | 8 | 125465736 | upstream gene variant | G/A;C;T | snv | 6 | |||||
rs998584 | 6 | 43790159 | downstream gene variant | C/A | snv | 0.41 | 4 | ||||
rs10769908 | 11 | 8462542 | intron variant | C/T | snv | 0.55 | 3 | ||||
rs9931989 | 16 | 28894763 | intron variant | G/C | snv | 0.68 | 3 | ||||
rs11231693 | 11 | 64095140 | intron variant | G/A | snv | 0.11 | 2 | ||||
rs1344674 | 3 | 141406344 | intron variant | A/G | snv | 0.55 | 2 | ||||
rs2745353 | 6 | 127131790 | intron variant | C/T | snv | 0.55 | 2 | ||||
rs987052 | 16 | 86288853 | intron variant | T/C | snv | 0.23 | 2 | ||||
rs1013443 | 5 | 180774114 | intergenic variant | A/T | snv | 1.4E-03 | 1 | ||||
rs1014242 | 7 | 32232693 | intron variant | C/T | snv | 0.54 | 1 | ||||
rs1021070 | 15 | 78654521 | intron variant | C/A;G | snv | 1 | |||||
rs1021071 | 15 | 78675837 | intron variant | G/C | snv | 0.28 | 1 | ||||
rs10226228 | 7 | 32276001 | intron variant | A/G | snv | 0.38 | 1 | ||||
rs10236197 | 7 | 32252149 | intron variant | T/C | snv | 0.41 | 1 | ||||
rs10259431 | 7 | 32241785 | intron variant | C/T | snv | 0.54 | 1 | ||||
rs10264177 | 7 | 32331250 | intron variant | A/G | snv | 0.40 | 1 | ||||
rs1028936 | 10 | 91590040 | regulatory region variant | A/C | snv | 0.18 | 1 | ||||
rs10951331 | 7 | 32314762 | intron variant | A/G | snv | 0.22 | 1 | ||||
rs10958725 | 8 | 42669441 | intergenic variant | T/G | snv | 0.63 | 1 | ||||
rs10958726 | 8 | 42680766 | intergenic variant | G/T | snv | 0.66 | 1 | ||||
rs11071927 | 15 | 66968834 | intergenic variant | C/A | snv | 0.85 | 1 | ||||
rs11072766 | 15 | 78479204 | intron variant | C/G;T | snv | 1 | |||||
rs11072774 | 15 | 78660355 | intron variant | C/T | snv | 0.20 | 1 | ||||
rs11072785 | 15 | 78675887 | intron variant | C/T | snv | 0.28 | 1 | ||||
rs11072787 | 15 | 78680635 | intron variant | T/C | snv | 0.34 | 1 |