Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
rs1799971 | 0.559 | 0.600 | 6 | 154039662 | missense variant | A/G | snv | 0.19 | 0.12 | 95 | |
rs4818 | 0.683 | 0.440 | 22 | 19963684 | synonymous variant | C/G;T | snv | 0.34 | 27 | ||
rs3745367 | 0.827 | 0.200 | 19 | 7669625 | intron variant | G/A | snv | 0.39 | 8 | ||
rs1718125 | 0.851 | 0.200 | 12 | 121155216 | intron variant | C/T | snv | 0.15 | 0.19 | 6 | |
rs373611092 | 0.925 | 0.160 | 22 | 19962794 | missense variant | A/G | snv | 8.4E-05 | 4.9E-05 | 5 | |
rs3845446 | 1 | 181797301 | intron variant | T/C | snv | 6.3E-02 | 3 | ||||
rs13080116 | 3 | 38865732 | intron variant | T/C | snv | 0.23 | 2 | ||||
rs33985936 | 3 | 38894643 | missense variant | C/A;T | snv | 8.0E-06; 0.22 | 2 | ||||
rs4286289 | 1.000 | 0.120 | 2 | 166305201 | intron variant | C/A | snv | 0.74 | 2 | ||
rs3732765 | 3 | 151372636 | missense variant | G/A | snv | 0.31 | 0.28 | 1 | |||
rs795484 | 12 | 118152057 | intron variant | T/C | snv | 0.71 | 1 |