Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10911362 | 1.000 | 0.040 | 1 | 183579857 | intron variant | A/G | snv | 0.12 | 1 | ||
rs10936599 | 0.637 | 0.600 | 3 | 169774313 | synonymous variant | C/T | snv | 0.29 | 0.21 | 32 | |
rs10956514 | 1.000 | 0.040 | 8 | 130240512 | intron variant | A/G | snv | 0.37 | 1 | ||
rs11012476 | 0.925 | 0.120 | 10 | 21003994 | intron variant | C/T | snv | 3.5E-02 | 3 | ||
rs1101998 | 1.000 | 0.040 | 1 | 159029494 | intron variant | C/T | snv | 0.65 | 1 | ||
rs11031728 | 1.000 | 0.040 | 11 | 32342070 | intron variant | C/G | snv | 0.18 | 1 | ||
rs11031731 | 0.925 | 0.040 | 11 | 32343884 | upstream gene variant | G/A | snv | 0.18 | 3 | ||
rs11040 | 1.000 | 0.040 | 6 | 81752132 | missense variant | C/A;G;T | snv | 1 | |||
rs11045819 | 0.851 | 0.120 | 12 | 21176879 | missense variant | C/A;T | snv | 0.11; 4.0E-06 | 4 | ||
rs11096957 | 0.790 | 0.160 | 4 | 38774870 | missense variant | T/G | snv | 0.42 | 0.41 | 8 | |
rs11117415 | 1.000 | 0.040 | 16 | 85917080 | intron variant | A/G | snv | 0.12 | 1 | ||
rs11246213 | 1.000 | 0.040 | 11 | 612967 | intron variant | A/G | snv | 0.25 | 0.33 | 1 | |
rs1128503 | 0.564 | 0.760 | 7 | 87550285 | synonymous variant | A/G | snv | 0.54 | 0.63 | 64 | |
rs1131454 | 0.882 | 0.040 | 12 | 112911065 | missense variant | G/A;C | snv | 0.57 | 3 | ||
rs1131498 | 0.732 | 0.360 | 1 | 169707345 | missense variant | A/G | snv | 0.21 | 0.22 | 13 | |
rs1135791 | 0.925 | 0.080 | 2 | 230177560 | missense variant | A/G | snv | 0.42 | 0.40 | 2 | |
rs11466617 | 1.000 | 0.040 | 4 | 38778850 | intron variant | T/C | snv | 0.13 | 2 | ||
rs11556887 | 1.000 | 0.040 | 2 | 230212961 | missense variant | G/A | snv | 0.10 | 7.4E-02 | 1 | |
rs11567764 | 1.000 | 0.040 | 5 | 35873503 | missense variant | G/A;T | snv | 9.5E-03; 4.0E-06 | 1 | ||
rs11575934 | 0.882 | 0.040 | 19 | 18075808 | missense variant | T/C | snv | 0.28 | 0.25 | 4 | |
rs11575935 | 0.925 | 0.040 | 19 | 18063921 | missense variant | C/T | snv | 1.1E-02 | 5.7E-03 | 2 | |
rs11674595 | 0.763 | 0.200 | 2 | 101994530 | intron variant | T/C | snv | 0.22 | 13 | ||
rs11774633 | 1.000 | 0.040 | 8 | 130177997 | intron variant | C/T | snv | 0.61 | 1 | ||
rs1190662183 | 1.000 | 0.040 | 19 | 10338932 | synonymous variant | C/T | snv | 1 | |||
rs11958933 | 1.000 | 0.040 | 5 | 25323598 | intron variant | G/A | snv | 0.70 | 1 |