Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1883349 | 1.000 | 22 | 43936063 | intron variant | G/A | snv | 0.19 | 1 | |||
rs2281298 | 1.000 | 22 | 43995354 | intron variant | G/A | snv | 0.21 | 1 | |||
rs926633 | 1.000 | 22 | 43941653 | intron variant | G/A | snv | 0.20 | 1 | |||
rs903361 | 0.882 | 0.160 | 1 | 203122146 | intron variant | G/A;C | snv | 4 | |||
rs12483959 | 1.000 | 22 | 43930116 | intron variant | G/A;C;T | snv | 4 | ||||
rs1572982 | 0.827 | 0.200 | 6 | 26094139 | intron variant | G/A;T | snv | 0.52; 8.0E-06 | 7 | ||
rs2294922 | 1.000 | 22 | 43983685 | intron variant | G/C | snv | 0.30 | 1 | |||
rs6006468 | 1.000 | 22 | 43987552 | non coding transcript exon variant | G/C | snv | 0.48 | 1 | |||
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 98 | ||
rs2401514 | 1.000 | 22 | 43998139 | intron variant | T/A | snv | 0.20 | 1 | |||
rs1007863 | 1.000 | 22 | 43999571 | missense variant | T/A;C | snv | 0.44 | 1 | |||
rs641738 | 0.689 | 0.320 | 19 | 54173068 | missense variant | T/A;C;G | snv | 22 | |||
rs2290602 | 0.882 | 0.040 | 4 | 23824109 | intron variant | T/A;G | snv | 3 | |||
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 62 | ||
rs17107315 | 0.620 | 0.440 | 5 | 147828115 | missense variant | T/C | snv | 9.1E-03 | 8.2E-03 | 40 | |
rs2126259 | 1.000 | 8 | 9327636 | intron variant | T/C | snv | 0.87 | 9 | |||
rs10499563 | 0.807 | 0.120 | 7 | 22720869 | intron variant | T/C | snv | 0.21 | 7 | ||
rs2071303 | 0.882 | 0.120 | 6 | 26091108 | splice region variant | T/C | snv | 0.38 | 0.36 | 6 | |
rs6601299 | 0.925 | 0.040 | 8 | 9327181 | intron variant | T/C | snv | 0.88 | 5 | ||
rs1010023 | 0.851 | 0.080 | 22 | 43940218 | intron variant | T/C | snv | 0.20 | 4 | ||
rs1474745 | 1.000 | 22 | 43953356 | intron variant | T/C | snv | 0.19 | 1 | |||
rs1883350 | 1.000 | 22 | 43932163 | intron variant | T/C | snv | 0.35 | 1 | |||
rs2073081 | 1.000 | 22 | 43939864 | intron variant | T/C | snv | 0.20 | 1 | |||
rs2235778 | 1.000 | 22 | 43993634 | intron variant | T/C | snv | 0.48 | 1 | |||
rs3827385 | 1.000 | 22 | 43992937 | intron variant | T/C | snv | 0.21 | 1 |