Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17782313 | 0.683 | 0.480 | 18 | 60183864 | intergenic variant | T/C | snv | 0.24 | 34 | ||
rs11206510 | 0.763 | 0.240 | 1 | 55030366 | intergenic variant | T/A;C;G | snv | 16 | |||
rs12970134 | 0.790 | 0.280 | 18 | 60217517 | intergenic variant | G/A | snv | 0.21 | 13 | ||
rs727428 | 0.882 | 0.200 | 17 | 7634474 | downstream gene variant | T/C | snv | 0.55 | 11 | ||
rs1111875 | 0.776 | 0.360 | 10 | 92703125 | intergenic variant | C/T | snv | 0.36 | 10 | ||
rs10830962 | 0.851 | 0.160 | 11 | 92965261 | upstream gene variant | C/A;G;T | snv | 7 | |||
rs1544210 | 0.882 | 0.240 | 10 | 92728044 | regulatory region variant | G/A | snv | 0.39 | 3 | ||
rs140485756 | 1.000 | 0.120 | 6 | 69410439 | intergenic variant | T/C | snv | 3.2E-02 | 2 | ||
rs2910397 | 1.000 | 0.120 | 19 | 47894860 | intergenic variant | C/T | snv | 0.38 | 2 | ||
rs56949836 | 1.000 | 0.120 | 9 | 90167763 | intergenic variant | C/T | snv | 8.9E-02 | 2 | ||
rs7312770 | 0.925 | 0.120 | 12 | 56073803 | upstream gene variant | C/T | snv | 0.53 | 2 | ||
rs74585555 | 1.000 | 0.120 | 2 | 81214976 | intergenic variant | G/A | snv | 4.9E-02 | 2 | ||
rs10739076 | 1.000 | 0.120 | 9 | 5440589 | upstream gene variant | A/C;T | snv | 1 | |||
rs10760321 | 1.000 | 0.120 | 9 | 124101917 | TF binding site variant | A/G | snv | 0.30 | 1 | ||
rs12460989 | 1.000 | 0.120 | 19 | 4785155 | non coding transcript exon variant | T/G | snv | 0.11 | 1 | ||
rs4744370 | 1.000 | 0.120 | 9 | 94715511 | intergenic variant | C/T | snv | 0.46 | 1 | ||
rs6022786 | 1.000 | 0.120 | 20 | 53830764 | upstream gene variant | A/G | snv | 0.55 | 1 | ||
rs684846 | 1.000 | 0.120 | 3 | 183173176 | downstream gene variant | C/T | snv | 0.85 | 1 | ||
rs7218361 | 1.000 | 0.120 | 17 | 39569151 | downstream gene variant | A/G | snv | 0.97 | 1 | ||
rs7558302 | 1.000 | 0.120 | 2 | 43609548 | TF binding site variant | C/T | snv | 0.59 | 1 | ||
rs7574059 | 1.000 | 0.120 | 2 | 123613428 | intergenic variant | G/A;C;T | snv | 1 | |||
rs8006998 | 1.000 | 0.120 | 14 | 75234687 | downstream gene variant | C/A;T | snv | 1 | |||
rs8013918 | 1.000 | 0.120 | 14 | 75242863 | intron variant | T/C | snv | 0.59 | 1 | ||
rs8013942 | 1.000 | 0.120 | 14 | 75244800 | intron variant | C/T | snv | 0.55 | 1 | ||
rs804279 | 1.000 | 0.120 | 8 | 11766380 | upstream gene variant | A/T | snv | 0.72 | 1 |