Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10795945 | 1.000 | 0.080 | 10 | 12260608 | intergenic variant | T/A;C | snv | 2 | |||
rs10811661 | 0.724 | 0.400 | 9 | 22134095 | intergenic variant | T/C | snv | 0.14 | 5 | ||
rs11257655 | 1.000 | 0.080 | 10 | 12265895 | TF binding site variant | C/T | snv | 0.23 | 4 | ||
rs12229654 | 0.763 | 0.320 | 12 | 110976657 | intergenic variant | T/G | snv | 4.8E-03 | 14 | ||
rs12970134 | 0.790 | 0.280 | 18 | 60217517 | intergenic variant | G/A | snv | 0.21 | 7 | ||
rs2191349 | 1.000 | 0.080 | 7 | 15024684 | intergenic variant | G/T | snv | 0.54 | 4 | ||
rs2867125 | 0.925 | 0.120 | 2 | 622827 | intergenic variant | T/A;C | snv | 0.85 | 6 | ||
rs2943634 | 0.763 | 0.200 | 2 | 226203364 | intergenic variant | A/C;G | snv | 8 | |||
rs562338 | 0.807 | 0.160 | 2 | 21065449 | intergenic variant | A/G | snv | 0.69 | 20 | ||
rs7020996 | 0.925 | 0.120 | 9 | 22129580 | downstream gene variant | C/A;T | snv | 3 | |||
rs7173964 | 1.000 | 0.080 | 15 | 62104743 | regulatory region variant | G/A | snv | 0.49 | 3 | ||
rs72892910 | 1.000 | 0.080 | 6 | 50849174 | downstream gene variant | G/T | snv | 0.17 | 2 | ||
rs7374732 | 1.000 | 0.080 | 3 | 23161963 | regulatory region variant | C/T | snv | 0.73 | 4 | ||
rs7923837 | 0.882 | 0.160 | 10 | 92722160 | intergenic variant | G/A;T | snv | 3 | |||
rs8089364 | 0.925 | 0.120 | 18 | 60191596 | upstream gene variant | T/C | snv | 0.21 | 6 | ||
rs11708067 | 0.882 | 0.080 | 3 | 123346931 | intron variant | A/G | snv | 0.19 | 6 | ||
rs4420638 | 0.708 | 0.520 | 19 | 44919689 | downstream gene variant | A/G | snv | 0.18 | 36 | ||
rs2246012 | 1.000 | 0.080 | 6 | 131577068 | intron variant | T/A;C | snv | 2 | |||
rs4865796 | 1.000 | 0.080 | 5 | 53976834 | intron variant | G/A | snv | 0.72 | 3 | ||
rs6947395 | 1.000 | 0.080 | 7 | 69941675 | intron variant | A/T | snv | 0.20 | 2 | ||
rs12454712 | 0.925 | 0.120 | 18 | 63178651 | intron variant | T/A;C | snv | 7 | |||
rs9891146 | 1.000 | 0.080 | 17 | 67991933 | missense variant | T/C | snv | 0.64 | 0.60 | 2 | |
rs76895963 | 1.000 | 0.080 | 12 | 4275678 | intron variant | T/G | snv | 1.5E-02 | 6 | ||
rs2206734 | 0.882 | 0.160 | 6 | 20694653 | intron variant | C/T | snv | 0.20 | 4 | ||
rs35261542 | 1.000 | 0.080 | 6 | 20675561 | intron variant | C/A | snv | 0.26 | 3 |