Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800587 | 0.620 | 0.720 | 2 | 112785383 | upstream gene variant | G/A;C | snv | 0.32 | 43 | ||
rs3783553 | 0.667 | 0.480 | 2 | 112774138 | 3 prime UTR variant | -/TGAA | delins | 26 | |||
rs17561 | 0.672 | 0.560 | 2 | 112779646 | missense variant | C/A | snv | 0.27 | 0.26 | 23 | |
rs2856836 | 0.763 | 0.280 | 2 | 112774506 | 3 prime UTR variant | A/G | snv | 0.26 | 9 | ||
rs3783521 | 0.807 | 0.200 | 2 | 112786000 | upstream gene variant | G/A | snv | 0.26 | 8 | ||
rs3783546 | 0.882 | 0.160 | 2 | 112777253 | intron variant | G/C | snv | 0.70 | 5 | ||
rs3783550 | 0.827 | 0.200 | 2 | 112775308 | intron variant | G/T | snv | 0.64 | 0.70 | 5 | |
rs2856838 | 0.851 | 0.200 | 2 | 112782395 | intron variant | G/A | snv | 0.37 | 4 | ||
rs1304037 | 0.882 | 0.200 | 2 | 112774659 | 3 prime UTR variant | T/C | snv | 0.32 | 3 | ||
rs1609682 | 0.882 | 0.160 | 2 | 112782628 | intron variant | G/T | snv | 0.70 | 3 | ||
rs113129609 | 0.925 | 0.080 | 2 | 112778091 | missense variant | A/G | snv | 2 | |||
rs1516792 | 0.925 | 0.080 | 2 | 112778356 | intron variant | G/A | snv | 2 | |||
rs16347 | 0.925 | 0.080 | 2 | 112774138 | 3 prime UTR variant | -/TGAA | delins | 0.70 | 2 | ||
rs1894399 | 0.925 | 0.040 | 2 | 112782600 | intron variant | C/T | snv | 0.32 | 2 | ||
rs1800794 | 1.000 | 0.040 | 2 | 112785696 | upstream gene variant | G/A | snv | 0.22 | 1 | ||
rs2071373 | 1.000 | 2 | 112782507 | intron variant | G/A | snv | 0.74 | 1 | |||
rs2071374 | 1.000 | 0.120 | 2 | 112779775 | intron variant | T/G | snv | 0.27 | 1 | ||
rs2071375 | 1.000 | 0.080 | 2 | 112777861 | intron variant | C/T | snv | 0.26 | 1 | ||
rs3783525 | 1.000 | 0.040 | 2 | 112784242 | intron variant | T/A;C | snv | 1 |