Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7138803 | 0.827 | 0.240 | 12 | 49853685 | intergenic variant | G/A;T | snv | 6 | |||
rs10808546 | 8 | 125483576 | intron variant | C/T | snv | 0.39 | 4 | ||||
rs605066 | 6 | 139508529 | intron variant | C/T | snv | 0.53 | 4 | ||||
rs998584 | 6 | 43790159 | downstream gene variant | C/A | snv | 0.41 | 4 | ||||
rs12936587 | 0.882 | 0.080 | 17 | 17640408 | regulatory region variant | G/A | snv | 0.38 | 3 | ||
rs13130484 | 1.000 | 0.080 | 4 | 45173674 | intergenic variant | C/A;T | snv | 3 | |||
rs6567160 | 1.000 | 0.080 | 18 | 60161902 | upstream gene variant | T/C | snv | 0.21 | 3 | ||
rs727428 | 0.882 | 0.200 | 17 | 7634474 | downstream gene variant | T/C | snv | 0.55 | 3 | ||
rs887912 | 1.000 | 0.080 | 2 | 59075742 | intron variant | T/C;G | snv | 3 | |||
rs10019888 | 4 | 26061368 | regulatory region variant | A/G | snv | 0.17 | 2 | ||||
rs12061508 | 1.000 | 0.040 | 1 | 196615338 | intergenic variant | G/A | snv | 0.23 | 2 | ||
rs12440695 | 15 | 62142957 | regulatory region variant | T/C | snv | 0.32 | 2 | ||||
rs12714415 | 2 | 651430 | intergenic variant | T/C | snv | 0.19 | 2 | ||||
rs1457489 | 1.000 | 0.080 | 18 | 60194728 | upstream gene variant | G/A | snv | 0.29 | 2 | ||
rs543874 | 1.000 | 0.080 | 1 | 177920345 | upstream gene variant | A/G | snv | 0.21 | 2 | ||
rs634869 | 6 | 139510620 | intron variant | T/A;C | snv | 2 | |||||
rs6905288 | 0.882 | 0.120 | 6 | 43791136 | downstream gene variant | G/A | snv | 0.56 | 2 | ||
rs1034207 | 6 | 127016554 | intron variant | C/A;G;T | snv | 0.94 | 1 | ||||
rs11154370 | 6 | 126846446 | intron variant | A/G;T | snv | 1 | |||||
rs1443512 | 12 | 53948900 | downstream gene variant | A/C;T | snv | 1 | |||||
rs17568628 | 5 | 76751114 | intergenic variant | T/C;G | snv | 1 | |||||
rs2119690 | 8 | 20002028 | intergenic variant | G/A;C | snv | 1 | |||||
rs2145272 | 20 | 6645571 | intergenic variant | G/A;T | snv | 1 | |||||
rs4580892 | 6 | 127088737 | intron variant | C/T | snv | 0.32 | 1 | ||||
rs4846567 | 1 | 219577375 | regulatory region variant | G/T | snv | 0.23 | 1 |