Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs997363 | 0.925 | 0.080 | 2 | 227644742 | intron variant | C/T | snv | 0.64 | 2 | ||
rs9931702 | 0.851 | 0.160 | 16 | 53492639 | non coding transcript exon variant | C/T | snv | 0.55 | 4 | ||
rs9917028 | 0.882 | 0.080 | 19 | 4640971 | non coding transcript exon variant | G/A | snv | 0.45 | 3 | ||
rs963918 | 0.827 | 0.120 | 14 | 68595397 | 3 prime UTR variant | C/T | snv | 0.64 | 5 | ||
rs963917 | 0.827 | 0.120 | 14 | 68595606 | 3 prime UTR variant | G/A | snv | 0.26 | 5 | ||
rs9532669 | 1.000 | 0.080 | 13 | 40927414 | downstream gene variant | A/T | snv | 0.51 | 1 | ||
rs953038635 | 0.590 | 0.800 | 6 | 159692720 | missense variant | G/A;T | snv | 8.0E-06 | 51 | ||
rs9513111 | 0.882 | 0.080 | 13 | 28423426 | intron variant | C/T | snv | 0.75 | 3 | ||
rs944309752 | 0.882 | 0.080 | 15 | 43421159 | synonymous variant | G/C | snv | 7.0E-06 | 3 | ||
rs9344 | 0.653 | 0.480 | 11 | 69648142 | splice region variant | G/A | snv | 0.45 | 0.39 | 34 | |
rs9302648 | 0.882 | 0.080 | 16 | 53493869 | non coding transcript exon variant | G/T | snv | 0.54 | 3 | ||
rs9298814 | 0.790 | 0.160 | 9 | 21227623 | missense variant | A/C;G | snv | 0.12; 8.8E-06 | 7 | ||
rs9277952 | 0.851 | 0.080 | 6 | 33236497 | upstream gene variant | G/A | snv | 0.10 | 4 | ||
rs9277535 | 0.724 | 0.440 | 6 | 33087084 | 3 prime UTR variant | A/G | snv | 0.25 | 13 | ||
rs9272143 | 0.882 | 0.080 | 6 | 32633026 | intron variant | T/C | snv | 0.49 | 3 | ||
rs920778 | 0.633 | 0.480 | 12 | 53966448 | intron variant | G/A | snv | 0.57 | 36 | ||
rs895819 | 0.623 | 0.560 | 19 | 13836478 | non coding transcript exon variant | T/A;C;G | snv | 0.34 | 0.38 | 46 | |
rs878854066 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 213 | |||
rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 104 | |
rs833070 | 0.776 | 0.440 | 6 | 43774889 | non coding transcript exon variant | T/C | snv | 0.58 | 11 | ||
rs833068 | 0.851 | 0.120 | 6 | 43774790 | non coding transcript exon variant | G/A | snv | 0.36 | 4 | ||
rs833061 | 0.605 | 0.600 | 6 | 43769749 | upstream gene variant | C/G;T | snv | 42 | |||
rs8305 | 0.882 | 0.120 | 18 | 54294435 | missense variant | G/A | snv | 0.72 | 0.78 | 4 | |
rs8179 | 0.882 | 0.080 | 7 | 92606850 | 3 prime UTR variant | T/A;C;G | snv | 8 | |||
rs8076131 | 0.790 | 0.200 | 17 | 39924659 | intron variant | G/A;C | snv | 11 |