Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs204991 | 0.882 | 0.200 | 6 | 32193589 | intron variant | T/C | snv | 0.21 | 3 | ||
rs204989 | 0.925 | 0.120 | 6 | 32194075 | intron variant | G/A | snv | 0.21 | 2 | ||
rs1385889785 | 1.000 | 0.040 | 1 | 157695436 | missense variant | G/C;T | snv | 4.0E-06; 4.0E-06 | 2 | ||
rs2234693 | 0.555 | 0.680 | 6 | 151842200 | intron variant | T/C | snv | 0.47 | 77 | ||
rs28936375 | 0.752 | 0.320 | 1 | 53197092 | missense variant | C/A | snv | 1.7E-04 | 2.2E-04 | 15 | |
rs1057519090 | 0.851 | 0.160 | 13 | 110492105 | missense variant | G/A | snv | 7 | |||
rs1057523354 | 0.763 | 0.480 | 13 | 110179387 | missense variant | C/A | snv | 13 | |||
rs35761398 | 0.701 | 0.520 | 1 | 23875429 | missense variant | TT/CC | mnv | 19 | |||
rs2501432 | 0.716 | 0.480 | 1 | 23875430 | missense variant | T/C;G | snv | 0.62 | 16 | ||
rs879761216 | 0.732 | 0.480 | 1 | 23875429 | frameshift variant | TT/C;T | delins | 14 | |||
rs6074028 | 1.000 | 0.040 | 20 | 46126219 | intron variant | A/C;G | snv | 1 | |||
rs73115010 | 1.000 | 0.040 | 20 | 46124597 | intron variant | T/C | snv | 0.18 | 1 | ||
rs13277113 | 0.695 | 0.520 | 8 | 11491677 | intron variant | G/A | snv | 0.25 | 18 | ||
rs7033979 | 0.925 | 0.040 | 9 | 92461698 | intron variant | A/G;T | snv | 2 | |||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 121 | |
rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 82 | |
rs1477353313 | 0.925 | 0.120 | 22 | 50744085 | missense variant | T/G | snv | 2 | |||
rs10499194 | 0.752 | 0.400 | 6 | 137681500 | intron variant | C/T | snv | 0.24 | 10 | ||
rs17197936 | 0.925 | 0.040 | 13 | 37601702 | upstream gene variant | T/C | snv | 5.2E-02 | 3 |