Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11740562 | 5 | 157515277 | intron variant | A/G | snv | 7.1E-02 | 2 | ||||
rs12745968 | 1 | 92936280 | intron variant | A/G | snv | 0.36 | 2 | ||||
rs5905512 | 1.000 | 0.040 | X | 43867148 | intron variant | A/G | snv | 2 | |||
rs6081541 | 1.000 | 0.040 | 20 | 19232246 | intron variant | A/G | snv | 0.20 | 2 | ||
rs4583255 | 16 | 29977620 | intron variant | A/G | snv | 0.36 | 1 | ||||
rs751229 | 1.000 | 0.040 | 1 | 231632793 | intron variant | A/G;T | snv | 2 | |||
rs2958182 | 0.882 | 0.040 | 18 | 55481790 | intron variant | A/T | snv | 0.72 | 5 | ||
rs165940 | 0.925 | 0.040 | 5 | 59383658 | intron variant | A/T | snv | 0.38 | 4 | ||
rs2619538 | 0.882 | 0.040 | 6 | 15664978 | upstream gene variant | A/T | snv | 0.54 | 4 | ||
rs17645023 | 1.000 | 0.040 | 17 | 66920916 | intergenic variant | A/T | snv | 0.22 | 3 | ||
rs3800373 | 0.752 | 0.200 | 6 | 35574699 | 3 prime UTR variant | C/A | snv | 0.68 | 22 | ||
rs1130214 | 0.742 | 0.280 | 14 | 104793397 | 5 prime UTR variant | C/A | snv | 0.31 | 12 | ||
rs1076560 | 0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 | 11 | ||
rs781720548 | 0.882 | 0.040 | 20 | 35652946 | stop gained | C/A | snv | 5 | |||
rs11789407 | 9 | 118597268 | intergenic variant | C/A | snv | 0.44 | 2 | ||||
rs3752088 | 1.000 | 0.040 | 18 | 50714891 | intron variant | C/A | snv | 0.51 | 2 | ||
rs6913660 | 1.000 | 0.040 | 6 | 27123646 | upstream gene variant | C/A | snv | 0.14 | 2 | ||
rs518147 | 0.807 | 0.200 | X | 114584109 | 5 prime UTR variant | C/A;G | snv | 7 | |||
rs2619539 | 0.925 | 0.040 | 6 | 15620624 | intron variant | C/A;G | snv | 3 | |||
rs893924483 | 0.716 | 0.280 | 11 | 27658285 | missense variant | C/A;T | snv | 4.0E-06 | 1.4E-05 | 23 | |
rs6994992 | 0.790 | 0.120 | 8 | 31638065 | upstream gene variant | C/A;T | snv | 13 | |||
rs2498804 | 0.827 | 0.160 | 14 | 104766758 | intron variant | C/A;T | snv | 0.40 | 0.33 | 8 | |
rs778293 | 0.807 | 0.120 | 13 | 105516850 | intergenic variant | C/A;T | snv | 7 | |||
rs778294 | 0.851 | 0.040 | 13 | 105489886 | synonymous variant | C/A;T | snv | 0.27; 4.0E-06 | 0.26 | 5 | |
rs2709722 | 1.000 | 0.040 | 7 | 20828189 | downstream gene variant | C/A;T | snv | 2 |