Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800795 | 0.494 | 0.840 | 7 | 22727026 | intron variant | C/G | snv | 0.71 | 140 | ||
rs1800896 | 0.507 | 0.800 | 1 | 206773552 | intron variant | T/C | snv | 0.41 | 113 | ||
rs505922 | 0.689 | 0.520 | 9 | 133273813 | intron variant | C/T | snv | 34 | |||
rs7804372 | 0.716 | 0.320 | 7 | 116554174 | intron variant | T/A | snv | 0.27 | 19 | ||
rs3807987 | 0.732 | 0.280 | 7 | 116539780 | intron variant | G/A | snv | 7.6E-02 | 17 | ||
rs1179251 | 0.763 | 0.320 | 12 | 68251271 | intron variant | C/G | snv | 0.18 | 14 | ||
rs10499563 | 0.807 | 0.120 | 7 | 22720869 | intron variant | T/C | snv | 0.21 | 7 | ||
rs12229892 | 0.807 | 0.240 | 12 | 112485589 | intron variant | G/A | snv | 1.4E-02 | 6 | ||
rs11536878 | 0.827 | 0.240 | 9 | 117709275 | intron variant | C/A | snv | 9.5E-02 | 5 | ||
rs158572 | 0.851 | 0.120 | 5 | 60943616 | intron variant | G/A | snv | 0.63 | 4 | ||
rs2301756 | 0.851 | 0.120 | 12 | 112452972 | intron variant | A/G | snv | 0.21 | 4 | ||
rs2709800 | 0.882 | 0.120 | 7 | 30473155 | intron variant | A/C | snv | 0.53 | 4 | ||
rs718226 | 0.882 | 0.120 | 16 | 50735652 | intron variant | A/G | snv | 0.36 | 4 | ||
rs1640827 | 0.882 | 0.120 | 1 | 223138265 | intron variant | C/G;T | snv | 3 | |||
rs17163737 | 0.882 | 0.120 | 1 | 223129809 | intron variant | G/T | snv | 7.2E-02 | 3 | ||
rs1878672 | 0.882 | 0.080 | 1 | 206770368 | intron variant | G/A;C;T | snv | 3 | |||
rs2015620 | 0.882 | 0.120 | 16 | 3073560 | intron variant | A/G;T | snv | 3 | |||
rs3805246 | 0.882 | 0.120 | 4 | 143382955 | intron variant | G/A | snv | 0.31 | 3 | ||
rs6912200 | 0.925 | 0.080 | 6 | 41750170 | intron variant | C/T | snv | 0.54 | 3 | ||
rs10420321 | 0.925 | 0.080 | 19 | 10189741 | intron variant | A/G | snv | 0.11 | 2 | ||
rs2243086 | 1.000 | 0.040 | 17 | 4930914 | intron variant | G/T | snv | 0.20 | 2 | ||
rs2376549 | 0.925 | 0.120 | 20 | 31411284 | intron variant | C/T | snv | 0.42 | 2 | ||
rs3024491 | 0.925 | 0.040 | 1 | 206771701 | intron variant | C/A;T | snv | 2 | |||
rs6490061 | 0.925 | 0.120 | 12 | 111335541 | intron variant | T/C | snv | 0.30 | 2 | ||
rs7205423 | 1.000 | 0.040 | 16 | 50735351 | intron variant | C/G;T | snv | 1 |