Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2555639 | 0.851 | 0.080 | 4 | 174540379 | non coding transcript exon variant | T/C | snv | 0.38 | 7 | ||
rs4464148 | 0.827 | 0.120 | 18 | 48932662 | intron variant | T/C | snv | 0.25 | 7 | ||
rs2270916 | 0.851 | 0.120 | 3 | 122282252 | intron variant | T/C | snv | 0.13 | 0.11 | 6 | |
rs60745952 | 0.925 | 0.080 | 4 | 148827842 | intron variant | T/C | snv | 0.13 | 6 | ||
rs2736118 | 0.882 | 0.120 | 5 | 1260080 | intron variant | T/C | snv | 0.33 | 4 | ||
rs2737 | 0.851 | 0.080 | 17 | 47981705 | missense variant | T/C | snv | 0.25 | 0.19 | 4 | |
rs2304204 | 0.882 | 0.160 | 19 | 49665763 | 5 prime UTR variant | T/C | snv | 0.39 | 3 | ||
rs4147542 | 0.882 | 0.160 | 4 | 99347396 | intron variant | T/C | snv | 0.33 | 3 | ||
rs6474387 | 0.882 | 0.080 | 8 | 42328734 | intron variant | T/C | snv | 0.76 | 3 | ||
rs1450640054 | 0.925 | 0.080 | 7 | 45921122 | missense variant | T/C | snv | 1.0E-05 | 2 | ||
rs17109924 | 0.925 | 0.080 | 12 | 71584007 | missense variant | T/C | snv | 7.4E-02 | 8.6E-02 | 2 | |
rs1724120 | 0.925 | 0.080 | 2 | 96143592 | 3 prime UTR variant | T/C | snv | 0.53 | 2 | ||
rs2099902 | 0.925 | 0.080 | 10 | 52766089 | 3 prime UTR variant | T/C | snv | 0.33 | 2 | ||
rs2470144 | 0.925 | 0.080 | 15 | 51329528 | intron variant | T/C | snv | 0.60 | 2 | ||
rs13181 | 0.487 | 0.760 | 19 | 45351661 | stop gained | T/A;G | snv | 4.0E-06; 0.32 | 134 | ||
rs459552 | 0.752 | 0.320 | 5 | 112841059 | missense variant | T/A;G | snv | 0.79 | 14 | ||
rs8905 | 0.925 | 0.080 | 17 | 68531661 | 3 prime UTR variant | T/A;G | snv | 2 | |||
rs1130409 | 0.555 | 0.720 | 14 | 20456995 | missense variant | T/A;C;G | snv | 4.0E-06; 4.0E-06; 0.42 | 72 | ||
rs2228612 | 0.763 | 0.160 | 19 | 10162696 | missense variant | T/A;C;G | snv | 0.14 | 12 | ||
rs4939827 | 0.708 | 0.160 | 18 | 48927093 | intron variant | T/A;C | snv | 25 | |||
rs1801155 | 0.649 | 0.440 | 5 | 112839514 | missense variant | T/A | snv | 8.0E-06; 2.0E-03 | 1.2E-03 | 42 | |
rs4696480 | 0.716 | 0.400 | 4 | 153685974 | intron variant | T/A | snv | 0.45 | 19 | ||
rs67376798 | 0.851 | 0.120 | 1 | 97082391 | missense variant | T/A | snv | 2.8E-03 | 3.3E-03 | 9 | |
rs1057519822 | 0.925 | 0.080 | 15 | 66481818 | missense variant | T/A | snv | 3 | |||
rs4648110 | 0.925 | 0.080 | 4 | 102612664 | intron variant | T/A | snv | 0.22 | 3 |