Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1024611 | 0.568 | 0.800 | 17 | 34252769 | upstream gene variant | A/G | snv | 0.28 | 63 | ||
rs8099917 | 0.581 | 0.600 | 19 | 39252525 | upstream gene variant | T/G | snv | 0.16 | 60 | ||
rs7652589 | 0.732 | 0.400 | 3 | 122170241 | downstream gene variant | A/G | snv | 0.60 | 13 | ||
rs7895833 | 0.742 | 0.440 | 10 | 67863299 | upstream gene variant | G/A;C | snv | 12 | |||
rs10937921 | 1.000 | 0.120 | 4 | 3274764 | downstream gene variant | C/T | snv | 0.40 | 2 | ||
rs1138690 | 1.000 | 0.120 | 4 | 3289674 | upstream gene variant | G/A;T | snv | 1 | |||
rs12668183 | 1.000 | 0.120 | 7 | 16455781 | regulatory region variant | T/C | snv | 0.34 | 1 | ||
rs7658462 | 1.000 | 0.120 | 4 | 3281695 | intergenic variant | C/T | snv | 0.16 | 1 | ||
rs1277892620 | 0.925 | 0.120 | 17 | 37242036 | synonymous variant | A/G | snv | 4.0E-06 | 7.0E-06 | 2 | |
rs762847 | 1.000 | 0.120 | 4 | 2910336 | intron variant | A/G | snv | 0.54 | 1 | ||
rs73786719 | 1.000 | 0.120 | 6 | 146716848 | intron variant | C/A | snv | 1.7E-02 | 3.3E-02 | 1 | |
rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 82 | |
rs2292779 | 0.851 | 0.320 | 8 | 140551294 | intron variant | G/C;T | snv | 0.57; 4.9E-06 | 4 | ||
rs4918 | 0.763 | 0.400 | 3 | 186620593 | missense variant | G/A;C | snv | 0.67 | 12 | ||
rs36117895 | 1.000 | 0.120 | 3 | 11358545 | missense variant | T/C | snv | 3.2E-02 | 3.9E-02 | 1 | |
rs1382597320 | 0.882 | 0.160 | 12 | 6934305 | missense variant | A/G | snv | 7.0E-06 | 3 | ||
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs1170668763 | 1.000 | 0.120 | 17 | 42818395 | missense variant | T/A | snv | 7.0E-06 | 1 | ||
rs756573441 | 1.000 | 0.120 | 7 | 134933359 | missense variant | A/G;T | snv | 4.2E-06 | 1 | ||
rs1801725 | 0.633 | 0.600 | 3 | 122284910 | missense variant | G/T | snv | 0.13 | 0.11 | 39 | |
rs3742330 | 0.662 | 0.640 | 14 | 95087025 | 3 prime UTR variant | A/G | snv | 8.7E-02 | 24 | ||
rs1057035 | 0.763 | 0.440 | 14 | 95087805 | 3 prime UTR variant | T/C | snv | 0.26 | 12 | ||
rs10719 | 0.677 | 0.680 | 5 | 31401340 | 3 prime UTR variant | A/G;T | snv | 0.69 | 24 | ||
rs644236 | 0.882 | 0.320 | 5 | 31409008 | non coding transcript exon variant | T/C | snv | 0.31 | 0.35 | 5 |