Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4129267 | 0.807 | 0.200 | 1 | 154453788 | intron variant | C/G;T | snv | 10 | |||
rs12239046 | 1 | 247438293 | intron variant | T/C | snv | 0.58 | 7 | ||||
rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 7 | ||
rs61812598 | 1.000 | 0.080 | 1 | 154447611 | intron variant | G/A | snv | 0.31 | 4 | ||
rs1892534 | 0.925 | 0.120 | 1 | 65640261 | 3 prime UTR variant | C/T | snv | 0.44 | 3 | ||
rs8192284 | 0.724 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 3 | |||
rs10489615 | 1 | 230169242 | intron variant | A/C;G | snv | 2 | |||||
rs11102001 | 0.925 | 0.080 | 1 | 109757069 | missense variant | G/A | snv | 9.4E-02 | 0.16 | 2 | |
rs10157379 | 1 | 247442297 | intron variant | C/G;T | snv | 1 | |||||
rs10864726 | 1 | 230160406 | intron variant | C/T | snv | 0.45 | 1 | ||||
rs1539019 | 0.882 | 0.240 | 1 | 247436999 | intron variant | A/C | snv | 0.63 | 1 | ||
rs1938492 | 1 | 65652146 | intergenic variant | A/C | snv | 0.43 | 1 | ||||
rs2376015 | 1 | 65658091 | intergenic variant | A/G | snv | 0.43 | 1 | ||||
rs4537545 | 0.790 | 0.160 | 1 | 154446403 | intron variant | C/T | snv | 0.48 | 1 | ||
rs4655582 | 1 | 65687680 | regulatory region variant | C/G | snv | 0.34 | 1 | ||||
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 25 | |
rs715 | 1.000 | 0.040 | 2 | 210678331 | 3 prime UTR variant | T/C | snv | 0.28 | 10 | ||
rs6734238 | 1.000 | 0.080 | 2 | 113083453 | upstream gene variant | A/G | snv | 0.39 | 5 | ||
rs7422339 | 1.000 | 0.080 | 2 | 210675783 | missense variant | C/A | snv | 5 | |||
rs7588285 | 2 | 3600596 | intron variant | C/G;T | snv | 3 | |||||
rs12712127 | 2 | 102110201 | intron variant | A/G | snv | 0.62 | 1 | ||||
rs1476698 | 2 | 241357034 | intron variant | A/G;T | snv | 1 | |||||
rs1558643 | 2 | 102115231 | intron variant | T/C;G | snv | 1 | |||||
rs59104589 | 2 | 241298487 | intron variant | C/T | snv | 0.30 | 1 | ||||
rs1154988 | 3 | 136206349 | upstream gene variant | T/A | snv | 0.76 | 5 |