Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs5186 | 0.630 | 0.560 | 3 | 148742201 | 3 prime UTR variant | A/C | snv | 0.23 | 0.21 | 38 | |
rs37369 | 0.807 | 0.120 | 5 | 35037010 | missense variant | C/T | snv | 0.21 | 0.25 | 9 | |
rs1332629192 | 0.851 | 0.200 | 4 | 73404374 | missense variant | C/T | snv | 7 | |||
rs136161 | 0.925 | 0.160 | 22 | 36261386 | intron variant | G/C | snv | 0.51 | 3 | ||
rs2276415 | 0.882 | 0.160 | 11 | 77590296 | missense variant | G/A | snv | 0.14 | 0.13 | 6 | |
rs121908117 | 0.708 | 0.440 | 3 | 48466707 | missense variant | G/A | snv | 17 | |||
rs739401 | 11 | 3015094 | intron variant | C/T | snv | 0.45 | 2 | ||||
rs7947841 | 11 | 34470133 | intron variant | G/A | snv | 1.0E-01 | 1 | ||||
rs1799864 | 0.572 | 0.680 | 3 | 46357717 | missense variant | G/A | snv | 0.13 | 0.12 | 68 | |
rs5443 | 0.532 | 0.760 | 12 | 6845711 | synonymous variant | C/T | snv | 0.36 | 0.44 | 106 | |
rs121913059 | 0.716 | 0.280 | 1 | 196747245 | missense variant | C/T | snv | 1.4E-04 | 1.9E-04 | 16 | |
rs6677604 | 0.827 | 0.200 | 1 | 196717788 | intron variant | G/A | snv | 0.23 | 7 | ||
rs55807605 | 1 | 196736919 | missense variant | G/A | snv | 1.4E-03 | 5.5E-04 | 1 | |||
rs57960694 | 1 | 196994083 | missense variant | G/A | snv | 1.1E-02 | 3.6E-02 | 1 | |||
rs267606743 | 1.000 | 0.160 | 13 | 110192222 | missense variant | C/T | snv | 5 | |||
rs1427118369 | 2 | 227283830 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 1 | |||
rs121912863 | 1.000 | 2 | 227008112 | missense variant | G/A | snv | 1.6E-04 | 1.8E-04 | 2 | ||
rs868580411 | 1.000 | X | 108602973 | missense variant | G/A;T | snv | 2 | ||||
rs763059810 | 0.623 | 0.600 | 2 | 136115750 | missense variant | T/C | snv | 4.0E-06 | 41 | ||
rs4740 | 0.827 | 0.240 | 19 | 4236999 | missense variant | G/A | snv | 0.34 | 0.39 | 8 | |
rs5370 | 0.630 | 0.520 | 6 | 12296022 | missense variant | G/T | snv | 0.23 | 0.21 | 37 | |
rs741301 | 0.925 | 0.160 | 7 | 36878390 | intron variant | C/T | snv | 0.59 | 3 | ||
rs1044498 | 0.752 | 0.360 | 6 | 131851228 | missense variant | A/C;G | snv | 0.19 | 15 | ||
rs1617640 | 0.742 | 0.520 | 7 | 100719675 | upstream gene variant | C/A;G;T | snv | 15 | |||
rs1799883 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 36 |