Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9917425 | 20 | 16755400 | intron variant | G/T | snv | 0.16 | 13 | ||||
rs11066301 | 0.827 | 0.200 | 12 | 112433568 | intron variant | A/G | snv | 0.30 | 12 | ||
rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 | |||
rs12041331 | 0.776 | 0.200 | 1 | 156899922 | intron variant | G/A | snv | 0.19 | 11 | ||
rs9494145 | 0.925 | 0.080 | 6 | 135111414 | intergenic variant | T/A;C | snv | 11 | |||
rs17758695 | 18 | 63253621 | intron variant | C/T | snv | 2.1E-02 | 10 | ||||
rs4895441 | 0.925 | 0.080 | 6 | 135105435 | upstream gene variant | A/G | snv | 0.21 | 10 | ||
rs739496 | 0.790 | 0.160 | 12 | 111449855 | 3 prime UTR variant | A/G | snv | 0.27 | 10 | ||
rs150813342 | 9 | 132989126 | synonymous variant | C/T | snv | 4.1E-03 | 4.1E-03 | 9 | |||
rs17145750 | 0.925 | 0.120 | 7 | 73612048 | intron variant | C/A;T | snv | 9 | |||
rs385893 | 0.925 | 0.080 | 9 | 4763176 | downstream gene variant | T/C | snv | 0.44 | 9 | ||
rs459193 | 0.925 | 0.120 | 5 | 56510924 | downstream gene variant | A/G | snv | 0.69 | 9 | ||
rs6993770 | 0.925 | 0.080 | 8 | 105569300 | intron variant | A/T | snv | 0.31 | 9 | ||
rs2075672 | 7 | 100642673 | intron variant | A/G | snv | 0.65 | 8 | ||||
rs3865444 | 0.851 | 0.160 | 19 | 51224706 | upstream gene variant | C/A | snv | 0.25 | 8 | ||
rs8037137 | 0.807 | 0.160 | 15 | 90963407 | upstream gene variant | T/C | snv | 0.19 | 8 | ||
rs1801689 | 17 | 66214462 | missense variant | A/C;G | snv | 4.0E-06; 2.4E-02; 4.8E-05 | 7 | ||||
rs2283847 | 22 | 27785411 | intron variant | C/A;G;T | snv | 7 | |||||
rs342293 | 0.882 | 0.040 | 7 | 106731773 | intron variant | C/G | snv | 0.42 | 7 | ||
rs3731211 | 9 | 21986848 | intron variant | T/A | snv | 0.74 | 7 | ||||
rs3747207 | 22 | 43928975 | intron variant | G/A | snv | 0.22 | 7 | ||||
rs9376090 | 6 | 135090090 | intron variant | T/C | snv | 0.19 | 7 | ||||
rs10761731 | 10 | 63267850 | intron variant | A/T | snv | 0.38 | 6 | ||||
rs11082304 | 18 | 23141009 | intron variant | G/C;T | snv | 6 | |||||
rs11553699 | 12 | 121779004 | 3 prime UTR variant | A/G | snv | 9.4E-02 | 6 |