Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10049390 | 0.776 | 0.080 | 3 | 133982275 | intron variant | G/A | snv | 0.67 | 10 | ||
rs1011970 | 0.677 | 0.320 | 9 | 22062135 | intron variant | G/T | snv | 0.23 | 22 | ||
rs10152518 | 0.790 | 0.080 | 15 | 67884824 | intergenic variant | G/A;T | snv | 9 | |||
rs1017621656 | 0.925 | 0.080 | 19 | 41352923 | missense variant | A/C;G | snv | 1.9E-05 | 3 | ||
rs1021631442 | 0.882 | 0.200 | 2 | 47806279 | missense variant | G/A | snv | 3 | |||
rs10222633 | 0.925 | 0.080 | 3 | 122258079 | intron variant | G/A | snv | 0.45 | 4 | ||
rs1028166 | 0.790 | 0.080 | 4 | 181892145 | intron variant | G/A | snv | 0.74 | 9 | ||
rs1035209 | 0.790 | 0.080 | 10 | 99585609 | intergenic variant | C/T | snv | 0.15 | 9 | ||
rs1039659576 | 0.689 | 0.520 | 1 | 236803473 | missense variant | A/G | snv | 21 | |||
rs10411210 | 0.742 | 0.160 | 19 | 33041394 | intron variant | C/T | snv | 0.22 | 13 | ||
rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
rs1042636 | 0.672 | 0.360 | 3 | 122284922 | missense variant | A/G | snv | 0.15 | 9.0E-02 | 23 | |
rs1042821 | 0.732 | 0.280 | 2 | 47783349 | missense variant | G/A;C;T | snv | 0.18; 8.6E-06 | 16 | ||
rs1044129 | 0.790 | 0.200 | 15 | 33866065 | 3 prime UTR variant | A/G;T | snv | 9 | |||
rs10450310 | 0.925 | 0.080 | 10 | 52764898 | downstream gene variant | G/A | snv | 0.29 | 2 | ||
rs1045485 | 0.637 | 0.480 | 2 | 201284866 | missense variant | G/A;C;T | snv | 4.0E-06; 9.0E-02 | 34 | ||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs10457678 | 0.790 | 0.080 | 6 | 138801103 | intron variant | A/G | snv | 0.19 | 10 | ||
rs104894226 | 0.658 | 0.560 | 11 | 534285 | missense variant | C/A;G;T | snv | 29 | |||
rs104894230 | 0.564 | 0.600 | 11 | 534288 | missense variant | C/A;G;T | snv | 73 | |||
rs10505477 | 0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 | 31 | ||
rs10506868 | 0.716 | 0.160 | 10 | 112559621 | intron variant | C/T | snv | 3.1E-02 | 16 | ||
rs10511330 | 0.776 | 0.080 | 3 | 114402172 | intron variant | T/C | snv | 0.22 | 10 | ||
rs1051753269 | 0.790 | 0.120 | 7 | 55174029 | missense variant | G/A | snv | 7.0E-06 | 7 | ||
rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 |