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 | |
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs1800497 | 0.620 | 0.400 | 11 | 113400106 | missense variant | G/A | snv | 0.26 | 0.26 | 56 | |
rs53576 | 0.641 | 0.320 | 3 | 8762685 | intron variant | A/G;T | snv | 42 | |||
rs2254298 | 0.701 | 0.200 | 3 | 8760542 | intron variant | G/A | snv | 0.16 | 23 | ||
rs13316193 | 0.882 | 0.040 | 3 | 8761057 | intron variant | T/C | snv | 0.45 | 4 | ||
rs237885 | 0.925 | 0.080 | 3 | 8753857 | intron variant | T/G | snv | 0.53 | 3 | ||
rs2268490 | 1.000 | 0.040 | 3 | 8755399 | intron variant | C/T | snv | 0.18 | 2 | ||
rs4686301 | 1.000 | 0.040 | 3 | 8756900 | intron variant | C/T | snv | 0.27 | 2 | ||
rs237887 | 1.000 | 0.040 | 3 | 8755356 | intron variant | G/A;C | snv | 2 | |||
rs1726886 | 12 | 44328993 | intron variant | G/A | snv | 0.67 | 1 |