Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs1800470 | 0.515 | 0.840 | 19 | 41353016 | missense variant | G/A;C | snv | 0.55; 2.4E-04 | 107 | ||
rs1800469 | 0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 | 78 | ||
rs121434568 | 0.568 | 0.560 | 7 | 55191822 | missense variant | T/A;G | snv | 73 | |||
rs1057519847 | 0.570 | 0.560 | 7 | 55191821 | missense variant | CT/AG | mnv | 72 | |||
rs1057519848 | 0.570 | 0.560 | 7 | 55191822 | missense variant | TG/GT | mnv | 72 | |||
rs121434569 | 0.581 | 0.520 | 7 | 55181378 | missense variant | C/T | snv | 2.8E-05 | 5.6E-05 | 70 | |
rs2241880 | 0.627 | 0.600 | 2 | 233274722 | missense variant | A/G | snv | 0.45 | 0.44 | 37 | |
rs121913227 | 0.653 | 0.320 | 7 | 140753336 | missense variant | AC/CT;TT | mnv | 31 | |||
rs1271572 | 0.708 | 0.400 | 14 | 64295199 | intron variant | A/C;T | snv | 16 | |||
rs2494732 | 0.763 | 0.240 | 14 | 104772855 | intron variant | T/C | snv | 0.50 | 0.47 | 11 | |
rs2699887 | 0.763 | 0.280 | 3 | 179148620 | intron variant | C/T | snv | 0.18 | 11 | ||
rs4803455 | 0.752 | 0.280 | 19 | 41345604 | intron variant | C/A | snv | 0.51 | 11 | ||
rs3809865 | 0.790 | 0.240 | 17 | 47311220 | 3 prime UTR variant | T/A;G | snv | 11 | |||
rs763538721 | 0.807 | 0.160 | 14 | 61740897 | missense variant | T/A | snv | 4.0E-06 | 8 | ||
rs751688663 | 0.807 | 0.280 | 3 | 11340656 | missense variant | G/A | snv | 4.0E-06 | 7 | ||
rs763375936 | 0.827 | 0.160 | 3 | 112532749 | missense variant | C/T | snv | 8.3E-06 | 7.0E-06 | 5 | |
rs772776695 | 0.827 | 0.160 | 3 | 112548576 | missense variant | T/A | snv | 4.0E-06 | 5 | ||
rs10036653 | 0.851 | 0.160 | 5 | 81970563 | upstream gene variant | A/T | snv | 0.17 | 4 | ||
rs3160 | 0.925 | 0.160 | 16 | 2209190 | 3 prime UTR variant | T/C | snv | 0.36 | 3 | ||
rs121913418 | 0.882 | 0.160 | 7 | 55174818 | missense variant | G/A;T | snv | 3 | |||
rs4760259 | 0.925 | 0.160 | 12 | 57467043 | intron variant | T/A;C | snv | 2 | |||
rs760112920 | 0.925 | 0.120 | 4 | 54731930 | missense variant | G/T | snv | 4.0E-06 | 3.5E-05 | 2 | |
rs26865 | 0.925 | 0.160 | 16 | 2203772 | upstream gene variant | A/G | snv | 0.41 | 2 |