Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10069690 | 0.595 | 0.560 | 5 | 1279675 | intron variant | C/T | snv | 0.36 | 19 | ||
rs10505477 | 0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 | 13 | ||
rs11651755 | 0.763 | 0.160 | 17 | 37739849 | intron variant | T/C | snv | 0.52 | 5 | ||
rs185229225 | 0.851 | 0.120 | 4 | 13607505 | intron variant | T/C | snv | 4 | |||
rs10088218 | 0.851 | 0.120 | 8 | 128531703 | intron variant | G/A | snv | 0.13 | 3 | ||
rs11782652 | 0.851 | 0.120 | 8 | 81741409 | intron variant | A/G | snv | 6.6E-02 | 3 | ||
rs1243180 | 0.790 | 0.160 | 10 | 21626690 | intron variant | T/A | snv | 0.23 | 3 | ||
rs13281615 | 0.716 | 0.360 | 8 | 127343372 | intron variant | A/G | snv | 0.43 | 3 | ||
rs2153271 | 0.925 | 0.160 | 9 | 16864523 | intron variant | C/T | snv | 0.43 | 3 | ||
rs2494938 | 0.752 | 0.240 | 6 | 40568389 | intron variant | G/A | snv | 0.51 | 3 | ||
rs2981582 | 0.695 | 0.360 | 10 | 121592803 | intron variant | A/G | snv | 0.58 | 3 | ||
rs757210 | 0.807 | 0.160 | 17 | 37736525 | intron variant | C/G;T | snv | 3 | |||
rs7651446 | 0.882 | 0.120 | 3 | 156689208 | intron variant | G/T | snv | 7.9E-02 | 3 | ||
rs9303542 | 0.882 | 0.120 | 17 | 48334138 | intron variant | A/G | snv | 0.34 | 3 | ||
rs17251221 | 0.724 | 0.360 | 3 | 122274400 | intron variant | A/G | snv | 0.11 | 2 | ||
rs2665390 | 0.776 | 0.160 | 3 | 156679960 | intron variant | C/T | snv | 0.92 | 2 | ||
rs34289250 | 0.925 | 0.120 | 17 | 61803285 | intron variant | T/C | snv | 7.8E-03 | 2 | ||
rs367899983 | 1.000 | 0.120 | 9 | 16864524 | intron variant | GTCT/- | delins | 4.2E-05 | 2 | ||
rs10756819 | 1.000 | 0.120 | 9 | 16858086 | intron variant | G/A;C;T | snv | 1 | |||
rs12373237 | 0.851 | 0.200 | 18 | 23845972 | intron variant | G/A | snv | 0.47 | 1 | ||
rs12379183 | 1.000 | 0.120 | 9 | 16865701 | intron variant | A/G | snv | 0.26 | 1 | ||
rs12379687 | 1.000 | 0.120 | 9 | 16854369 | intron variant | G/A;T | snv | 1 | |||
rs12451939 | 1.000 | 0.120 | 17 | 61970281 | intron variant | A/G | snv | 2.6E-02 | 1 | ||
rs1256030 | 0.827 | 0.240 | 14 | 64280452 | intron variant | A/G;T | snv | 1 | |||
rs1256031 | 0.790 | 0.200 | 14 | 64279461 | intron variant | G/A;T | snv | 0.57 | 1 |