Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11191580 | 0.827 | 0.040 | 10 | 103146454 | intron variant | T/C | snv | 7.9E-02 | 12 | ||
rs174576 | 0.851 | 0.200 | 11 | 61836038 | intron variant | C/A;T | snv | 12 | |||
rs1333048 | 0.683 | 0.320 | 9 | 22125348 | intron variant | A/C | snv | 0.44 | 10 | ||
rs1480380 | 0.763 | 0.360 | 6 | 32945469 | intron variant | C/T | snv | 0.11 | 10 | ||
rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 7 | ||
rs1516725 | 0.925 | 0.120 | 3 | 186106215 | intron variant | T/C | snv | 0.86 | 7 | ||
rs2710323 | 0.851 | 0.080 | 3 | 52781889 | intron variant | T/C | snv | 0.49 | 0.54 | 7 | |
rs12576775 | 0.827 | 0.080 | 11 | 79366149 | intron variant | A/G | snv | 0.15 | 6 | ||
rs2252865 | 0.851 | 0.040 | 1 | 8362616 | intron variant | T/C | snv | 0.72 | 6 | ||
rs9371601 | 0.790 | 0.120 | 6 | 152469438 | intron variant | G/T | snv | 0.46 | 6 | ||
rs10275045 | 0.882 | 0.160 | 7 | 1881190 | intron variant | C/T | snv | 0.35 | 5 | ||
rs10503253 | 0.851 | 0.040 | 8 | 4323322 | intron variant | C/A | snv | 0.18 | 5 | ||
rs10994359 | 0.827 | 0.040 | 10 | 60462349 | intron variant | T/C | snv | 8.0E-02 | 5 | ||
rs10994397 | 0.851 | 0.040 | 10 | 60519366 | intron variant | C/T | snv | 9.5E-02 | 5 | ||
rs11152369 | 0.851 | 0.040 | 18 | 55399097 | intron variant | A/C | snv | 6.3E-02 | 5 | ||
rs11191454 | 0.776 | 0.160 | 10 | 102900247 | intron variant | A/G | snv | 7.9E-02 | 5 | ||
rs12325410 | 0.851 | 0.040 | 16 | 9581389 | intron variant | T/G | snv | 0.16 | 5 | ||
rs12443954 | 0.851 | 0.040 | 16 | 89675088 | intron variant | A/C;G | snv | 5 | |||
rs1625579 | 0.763 | 0.160 | 1 | 98037378 | intron variant | G/T | snv | 0.78 | 5 | ||
rs2021722 | 0.851 | 0.040 | 6 | 30206354 | intron variant | C/A;T | snv | 0.24 | 5 | ||
rs2388334 | 0.882 | 0.040 | 6 | 98143746 | intron variant | A/G | snv | 0.39 | 5 | ||
rs2535629 | 0.827 | 0.040 | 3 | 52799203 | intron variant | G/A;C | snv | 5 | |||
rs2721800 | 0.851 | 0.040 | 7 | 24652933 | intron variant | G/A;C;T | snv | 5 | |||
rs2799573 | 0.851 | 0.040 | 10 | 18312999 | intron variant | T/C | snv | 0.20 | 5 | ||
rs28456 | 0.925 | 0.120 | 11 | 61822009 | intron variant | A/C;G | snv | 5 |