Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 98 | ||
rs2075650 | 0.662 | 0.360 | 19 | 44892362 | intron variant | A/G | snv | 0.13 | 0.13 | 45 | |
rs2074356 | 0.763 | 0.280 | 12 | 112207597 | intron variant | G/A | snv | 3.8E-03 | 18 | ||
rs301806 | 0.851 | 0.120 | 1 | 8422018 | intron variant | C/T | snv | 0.62 | 6 | ||
rs10462028 | 0.882 | 0.120 | 4 | 55432133 | 3 prime UTR variant | G/A | snv | 0.28 | 4 | ||
rs34668726 | 1.000 | 0.040 | 2 | 23673031 | intron variant | C/G | snv | 0.13 | 3 |