Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10811661 | 0.724 | 0.400 | 9 | 22134095 | intergenic variant | T/C | snv | 0.14 | 22 | ||
rs1111875 | 0.776 | 0.360 | 10 | 92703125 | intergenic variant | C/T | snv | 0.36 | 10 | ||
rs17446593 | 1.000 | 0.080 | 13 | 40553948 | intron variant | A/G | snv | 0.19 | 2 | ||
rs3851179 | 0.752 | 0.280 | 11 | 86157598 | downstream gene variant | T/C | snv | 0.70 | 15 | ||
rs744373 | 0.851 | 0.160 | 2 | 127137039 | downstream gene variant | A/G | snv | 0.35 | 8 | ||
rs11061946 | 1.000 | 0.080 | 12 | 1719361 | intron variant | C/T | snv | 6.8E-02 | 2 | ||
rs11061973 | 1.000 | 0.080 | 12 | 1756770 | intron variant | G/A | snv | 0.12 | 2 | ||
rs1042714 | 0.597 | 0.640 | 5 | 148826910 | stop gained | G/C;T | snv | 0.68 | 54 | ||
rs4994 | 0.578 | 0.640 | 8 | 37966280 | missense variant | A/G | snv | 0.11 | 9.2E-02 | 65 | |
rs2278426 | 1.000 | 0.080 | 19 | 11239812 | missense variant | C/T | snv | 0.11 | 0.11 | 11 | |
rs945508 | 1.000 | 0.080 | 1 | 156937289 | missense variant | T/C | snv | 0.64 | 0.66 | 3 | |
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs3731201 | 1.000 | 0.080 | 9 | 21988897 | intron variant | C/T | snv | 0.86 | 2 | ||
rs495490 | 1.000 | 0.080 | 9 | 22010413 | intron variant | A/G | snv | 6.8E-02 | 2 | ||
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs997509 | 0.827 | 0.200 | 6 | 131846837 | intron variant | C/T | snv | 5.3E-02 | 6 | ||
rs1799883 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 36 | ||
rs17446614 | 0.851 | 0.240 | 13 | 40565740 | intron variant | G/A | snv | 0.16 | 5 | ||
rs2297627 | 0.925 | 0.120 | 13 | 40659794 | intron variant | A/G | snv | 0.41 | 3 | ||
rs2721068 | 0.882 | 0.160 | 13 | 40565575 | intron variant | T/C | snv | 0.38 | 4 | ||
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 98 | ||
rs1801483 | 0.851 | 0.160 | 17 | 81809839 | missense variant | G/A | snv | 7.4E-03 | 6.3E-03 | 7 | |
rs773641005 | 0.742 | 0.240 | 16 | 58723829 | missense variant | T/C | snv | 14 | |||
rs1169288 | 0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 | 21 | ||
rs3813929 | 0.851 | 0.240 | X | 114584047 | upstream gene variant | C/G;T | snv | 5 |