Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs939317 | 3 | 184328011 | intron variant | A/C;G | snv | 0.76 | 0.80 | 1 | |||
rs3914188 | 3 | 184292260 | 3 prime UTR variant | G/C | snv | 0.73 | 0.73 | 2 | |||
rs1131017 | 0.925 | 0.160 | 12 | 56042145 | 5 prime UTR variant | C/A;G;T | snv | 8.0E-06; 8.0E-06; 0.62; 1.1E-04 | 5 | ||
rs1933437 | 13 | 28050157 | missense variant | G/A | snv | 0.60 | 0.53 | 2 | |||
rs999885 | 0.925 | 0.120 | 7 | 100103553 | intron variant | G/A | snv | 0.56 | 0.46 | 3 | |
rs365132 | 5 | 176951573 | synonymous variant | G/T | snv | 0.51 | 0.58 | 2 | |||
rs2725405 | 17 | 81246424 | missense variant | G/C | snv | 0.49 | 0.36 | 1 | |||
rs2297605 | 9 | 124493169 | intron variant | G/A;C;T | snv | 0.49; 3.7E-05; 8.2E-06 | 1 | ||||
rs9652589 | 16 | 20359494 | missense variant | C/T | snv | 0.44 | 0.46 | 2 | |||
rs913588 | 9 | 7174673 | missense variant | G/A | snv | 0.42 | 0.43 | 1 | |||
rs707938 | 6 | 31761582 | synonymous variant | A/G | snv | 0.38 | 0.44 | 3 | |||
rs2836950 | 21 | 39232503 | splice region variant | C/A;G | snv | 9.0E-06; 0.37 | 1 | ||||
rs1799949 | 17 | 43093449 | synonymous variant | G/A | snv | 0.35 | 0.31 | 2 | |||
rs5742915 | 0.925 | 0.080 | 15 | 74044292 | missense variant | T/C;G | snv | 0.35; 4.0E-06 | 7 | ||
rs66461782 | 1 | 71067604 | intron variant | A/T | snv | 0.32 | 0.27 | 2 | |||
rs4889 | 0.882 | 0.160 | 1 | 204190659 | missense variant | G/A;C | snv | 5.2E-06; 0.29 | 5 | ||
rs3133974 | 8 | 93734470 | synonymous variant | G/A;C;T | snv | 2.6E-04; 4.0E-06; 9.2E-05; 0.28 | 1 | ||||
rs11556924 | 0.752 | 0.240 | 7 | 130023656 | missense variant | C/A;T | snv | 4.0E-06; 0.28 | 21 | ||
rs34811474 | 1.000 | 0.040 | 4 | 25407216 | missense variant | G/A;T | snv | 0.15; 4.1E-06 | 8 | ||
rs3746619 | 0.925 | 0.200 | 20 | 56248749 | 5 prime UTR variant | C/A | snv | 0.14 | 0.21 | 3 | |
rs2277339 | 12 | 56752285 | missense variant | T/G | snv | 0.12 | 0.14 | 10 | |||
rs17854357 | 11 | 65834089 | splice region variant | G/C;T | snv | 0.12; 5.8E-05 | 1 | ||||
rs61744130 | 19 | 53576813 | missense variant | T/C | snv | 5.9E-02 | 3.9E-02 | 1 | |||
rs80170948 | 5 | 64724489 | missense variant | T/G | snv | 3.0E-02 | 2.8E-02 | 2 | |||
rs72661148 | 18 | 47845324 | synonymous variant | A/G | snv | 2.2E-02 | 2.4E-02 | 1 |