Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2243086 | 1.000 | 0.040 | 17 | 4930914 | intron variant | G/T | snv | 0.20 | 2 | ||
rs3024491 | 0.925 | 0.040 | 1 | 206771701 | intron variant | C/A;T | snv | 2 | |||
rs1402686368 | 1.000 | 0.040 | 7 | 101133793 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs7205423 | 1.000 | 0.040 | 16 | 50735351 | intron variant | C/G;T | snv | 1 | |||
rs8111085 | 1.000 | 0.040 | 19 | 10162696 | missense variant | T/A;C;G | snv | 1 | |||
rs1878672 | 0.882 | 0.080 | 1 | 206770368 | intron variant | G/A;C;T | snv | 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 | ||
rs10499563 | 0.807 | 0.120 | 7 | 22720869 | intron variant | T/C | snv | 0.21 | 7 | ||
rs158572 | 0.851 | 0.120 | 5 | 60943616 | intron variant | G/A | snv | 0.63 | 4 | ||
rs1917799 | 0.851 | 0.120 | 10 | 49542929 | upstream gene variant | A/C | snv | 0.25 | 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 | ||
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 | ||
rs1330344 | 0.925 | 0.120 | 9 | 122369409 | upstream gene variant | C/T | snv | 0.69 | 2 | ||
rs2376549 | 0.925 | 0.120 | 20 | 31411284 | intron variant | C/T | snv | 0.42 | 2 | ||
rs6490061 | 0.925 | 0.120 | 12 | 111335541 | intron variant | T/C | snv | 0.30 | 2 | ||
rs2066842 | 0.763 | 0.200 | 16 | 50710713 | missense variant | C/A;T | snv | 4.0E-06; 0.19 | 15 | ||
rs2075820 | 0.790 | 0.200 | 7 | 30452621 | missense variant | C/T | snv | 0.27 | 0.28 | 10 | |
rs3024496 | 0.827 | 0.200 | 1 | 206768519 | 3 prime UTR variant | A/G | snv | 0.43 | 6 | ||
rs12229892 | 0.807 | 0.240 | 12 | 112485589 | intron variant | G/A | snv | 1.4E-02 | 6 |