Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10146249 | 1.000 | 0.080 | 14 | 92074996 | intron variant | C/A | snv | 0.29 | 1 | ||
rs26311 | 1.000 | 0.080 | 3 | 10291242 | 5 prime UTR variant | C/G | snv | 0.16 | 1 | ||
rs3017895 | 1.000 | 0.080 | 4 | 88728340 | 3 prime UTR variant | A/G | snv | 0.19 | 1 | ||
rs3730017 | 1.000 | 0.080 | 17 | 27782076 | missense variant | G/A | snv | 3.7E-02 | 7.2E-02 | 1 | |
rs7158733 | 1.000 | 0.080 | 14 | 92070879 | stop gained | G/A;T | snv | 1.2E-05; 0.27 | 1 | ||
rs886277 | 1.000 | 0.080 | 11 | 2418537 | missense variant | T/C | snv | 0.44 | 0.47 | 1 | |
rs1049305 | 0.925 | 0.160 | 7 | 30924207 | 3 prime UTR variant | G/C | snv | 0.52 | 4 | ||
rs10020432 | 0.925 | 0.080 | 4 | 73455883 | 3 prime UTR variant | A/G | snv | 0.54 | 2 | ||
rs1140409 | 0.925 | 0.080 | 17 | 64500552 | missense variant | A/C | snv | 5.4E-02 | 5.0E-02 | 2 | |
rs1201810520 | 0.925 | 0.160 | 2 | 88590497 | missense variant | C/T | snv | 2 | |||
rs12104272 | 0.925 | 0.080 | 19 | 49644795 | intron variant | G/A | snv | 0.44 | 2 | ||
rs1227756 | 0.925 | 0.080 | 10 | 69828748 | intron variant | G/A;C | snv | 2 | |||
rs1469557 | 0.925 | 0.120 | 8 | 10849291 | downstream gene variant | C/T | snv | 0.18 | 2 | ||
rs1545224 | 0.925 | 0.120 | 2 | 88124297 | 3 prime UTR variant | A/G | snv | 0.18 | 2 | ||
rs2298839 | 0.925 | 0.080 | 4 | 73445127 | splice region variant | A/G;T | snv | 0.54 | 2 | ||
rs2629751 | 0.925 | 0.120 | 12 | 104028030 | intron variant | A/G | snv | 0.36 | 2 | ||
rs2679757 | 0.925 | 0.080 | 8 | 102858590 | intron variant | A/G | snv | 0.37 | 2 | ||
rs2710833 | 0.925 | 0.080 | 4 | 168488807 | intron variant | T/A;C | snv | 2 | |||
rs343064 | 0.925 | 0.080 | 7 | 35515178 | upstream gene variant | C/G;T | snv | 2 | |||
rs4646038 | 0.925 | 0.080 | 1 | 15506705 | intron variant | C/T | snv | 7.0E-06 | 2 | ||
rs571462252 | 0.925 | 0.080 | 12 | 52904720 | missense variant | G/A | snv | 2 | |||
rs642588 | 0.925 | 0.120 | 6 | 159990235 | intron variant | A/G | snv | 0.83 | 2 | ||
rs643608 | 0.925 | 0.080 | 21 | 43348682 | intergenic variant | C/T | snv | 0.69 | 2 | ||
rs6487679 | 0.925 | 0.080 | 12 | 9218736 | intergenic variant | C/T | snv | 0.80 | 2 | ||
rs6591182 | 0.925 | 0.080 | 11 | 65582285 | missense variant | T/G | snv | 0.47 | 0.45 | 2 |