Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1341667 | 0.925 | 0.040 | 10 | 68882104 | missense variant | T/C | snv | 0.62 | 0.57 | 4 | |
rs2507800 | 1.000 | 0.040 | 8 | 107250441 | 3 prime UTR variant | T/A | snv | 0.36 | 2 | ||
rs7576192 | 1.000 | 0.040 | 2 | 120360455 | intergenic variant | A/G | snv | 0.68 | 2 | ||
rs7579169 | 1.000 | 0.040 | 2 | 120360548 | intergenic variant | T/C | snv | 0.68 | 2 | ||
rs2198532 | 1.000 | 0.040 | 2 | 3827777 | intron variant | T/C | snv | 0.79 | 1 | ||
rs7020782 | 1.000 | 0.040 | 9 | 116344602 | missense variant | C/A | snv | 0.68 | 0.59 | 1 | |
rs770016471 | 1.000 | 0.040 | 17 | 63497260 | missense variant | C/G | snv | 1.4E-05 | 1 | ||
rs779370907 | 1.000 | 0.040 | 19 | 18436405 | synonymous variant | C/T | snv | 6.0E-05 | 1.4E-05 | 1 | |
rs780972489 | 1.000 | 0.040 | 19 | 18436831 | synonymous variant | C/T | snv | 8.9E-06 | 7.0E-06 | 1 | |
rs1800595 | 0.925 | 0.080 | 1 | 169541110 | missense variant | T/C;G | snv | 5.7E-02 | 2 | ||
rs3756261 | 0.925 | 0.160 | 4 | 109911150 | upstream gene variant | T/C | snv | 9.9E-02 | 2 | ||
rs1177506410 | 0.776 | 0.240 | 1 | 230706148 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 12 | |
rs1275805226 | 0.776 | 0.240 | 1 | 230706148 | frameshift variant | G/- | del | 7.0E-06 | 12 | ||
rs2059806 | 0.807 | 0.240 | 19 | 7166365 | synonymous variant | C/G;T | snv | 4.0E-06; 0.26 | 7 | ||
rs2536512 | 0.752 | 0.280 | 4 | 24799693 | missense variant | G/A;T | snv | 0.55 | 14 | ||
rs11549467 | 0.653 | 0.400 | 14 | 61740857 | missense variant | G/A | snv | 8.9E-03 | 7.0E-03 | 30 | |
rs4762 | 0.637 | 0.440 | 1 | 230710231 | missense variant | G/A | snv | 0.12 | 0.11 | 35 | |
rs2890565 | 0.732 | 0.440 | 1 | 7849677 | missense variant | C/T | snv | 8.7E-02 | 5.6E-02 | 15 | |
rs268 | 0.637 | 0.480 | 8 | 19956018 | missense variant | A/G | snv | 1.3E-02 | 1.3E-02 | 41 | |
rs5370 | 0.630 | 0.520 | 6 | 12296022 | missense variant | G/T | snv | 0.23 | 0.21 | 37 | |
rs351855 | 0.597 | 0.560 | 5 | 177093242 | missense variant | G/A | snv | 0.33 | 0.26 | 58 | |
rs6025 | 0.637 | 0.560 | 1 | 169549811 | missense variant | C/T | snv | 1.8E-02 | 43 | ||
rs1799889 | 0.649 | 0.600 | 7 | 101126430 | upstream gene variant | A/G | snv | 31 | |||
rs2234693 | 0.555 | 0.680 | 6 | 151842200 | intron variant | T/C | snv | 0.47 | 77 | ||
rs9340799 | 0.583 | 0.680 | 6 | 151842246 | intron variant | A/G | snv | 0.32 | 62 |