Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10213865 | 0.827 | 0.120 | 5 | 35857748 | intron variant | A/C;T | snv | 5 | |||
rs1026411 | 0.827 | 0.080 | 8 | 127014165 | intron variant | G/A;C | snv | 0.25 | 5 | ||
rs104886026 | 0.851 | 0.080 | 7 | 55200333 | missense variant | G/A | snv | 4 | |||
rs1051753269 | 0.790 | 0.120 | 7 | 55174029 | missense variant | G/A | snv | 7.0E-06 | 7 | ||
rs1056836 | 0.581 | 0.680 | 2 | 38071060 | missense variant | G/C | snv | 0.51 | 58 | ||
rs1057519784 | 0.827 | 0.080 | 2 | 29220765 | missense variant | G/T | snv | 7 | |||
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 | |||
rs1057519861 | 0.776 | 0.080 | 7 | 55181398 | missense variant | T/A | snv | 15 | |||
rs1057519975 | 0.649 | 0.480 | 17 | 7675209 | missense variant | A/C;G;T | snv | 34 | |||
rs1062980 | 0.827 | 0.080 | 15 | 78500185 | 3 prime UTR variant | T/C | snv | 0.39 | 8 | ||
rs1064607 | 0.827 | 0.200 | 3 | 188877884 | 3 prime UTR variant | G/C | snv | 0.46 | 5 | ||
rs10877887 | 0.701 | 0.440 | 12 | 62603400 | non coding transcript exon variant | T/C | snv | 0.42 | 18 | ||
rs10937405 | 0.807 | 0.080 | 3 | 189665394 | intron variant | C/T | snv | 0.38 | 9 | ||
rs1131691014 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 214 | |||
rs11568820 | 0.672 | 0.480 | 12 | 47908762 | intron variant | C/T | snv | 0.38 | 27 | ||
rs121434568 | 0.568 | 0.560 | 7 | 55191822 | missense variant | T/A;G | snv | 73 | |||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs121913465 | 0.763 | 0.160 | 7 | 55181312 | missense variant | G/T | snv | 11 | |||
rs121913469 | 0.763 | 0.240 | 17 | 39723966 | missense variant | TT/CC | mnv | 11 | |||
rs121913530 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 63 | |||
rs1258159645 | 0.630 | 0.600 | 16 | 69711128 | missense variant | G/A | snv | 7.0E-06 | 37 | ||
rs1275824108 | 0.851 | 0.080 | 14 | 54399922 | missense variant | A/G | snv | 7.0E-06 | 5 | ||
rs12910984 | 0.827 | 0.080 | 15 | 78599285 | intron variant | G/A;C;T | snv | 8 | |||
rs12914385 | 0.790 | 0.160 | 15 | 78606381 | intron variant | C/A;T | snv | 18 |