Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs75030001 | 0.807 | 0.160 | 10 | 43118458 | missense variant | G/C;T | snv | 4.0E-06; 2.0E-05 | 4 | ||
rs965513 | 0.742 | 0.200 | 9 | 97793827 | intron variant | A/G;T | snv | 4 | |||
rs10741657 | 0.637 | 0.520 | 11 | 14893332 | upstream gene variant | A/G | snv | 0.65 | 3 | ||
rs116909374 | 0.776 | 0.120 | 14 | 36269155 | regulatory region variant | C/T | snv | 2.3E-02 | 3 | ||
rs121913238 | 0.732 | 0.240 | 12 | 25227343 | missense variant | G/C;T | snv | 3 | |||
rs121913254 | 0.658 | 0.440 | 1 | 114713909 | stop gained | G/A;C;T | snv | 3 | |||
rs1447295 | 0.658 | 0.400 | 8 | 127472793 | intron variant | A/C;T | snv | 3 | |||
rs1801516 | 0.627 | 0.400 | 11 | 108304735 | missense variant | G/A | snv | 0.11 | 0.11 | 3 | |
rs2622590 | 0.925 | 0.080 | 8 | 55445714 | intron variant | G/A | snv | 0.15 | 3 | ||
rs4915076 | 0.882 | 0.080 | 1 | 107816883 | intron variant | T/C | snv | 9.1E-02 | 3 | ||
rs11175834 | 0.925 | 0.080 | 12 | 65598856 | intron variant | C/T | snv | 0.14 | 2 | ||
rs1143627 | 0.605 | 0.760 | 2 | 112836810 | 5 prime UTR variant | G/A | snv | 0.56 | 2 | ||
rs12990503 | 0.925 | 0.080 | 2 | 217429494 | intron variant | C/G | snv | 0.64 | 2 | ||
rs1562430 | 0.807 | 0.160 | 8 | 127375606 | intron variant | T/C | snv | 0.41 | 2 | ||
rs1566734 | 0.807 | 0.120 | 11 | 48123823 | missense variant | A/C | snv | 0.17 | 0.15 | 2 | |
rs1874564 | 0.925 | 0.080 | 4 | 76936952 | intergenic variant | G/A | snv | 0.58 | 2 | ||
rs2069837 | 0.724 | 0.520 | 7 | 22728408 | intron variant | A/C;G | snv | 2 | |||
rs2736098 | 0.600 | 0.600 | 5 | 1293971 | synonymous variant | C/T | snv | 0.29 | 0.22 | 2 | |
rs4649295 | 0.925 | 0.080 | 1 | 233280792 | intron variant | T/C | snv | 0.60 | 2 | ||
rs6996585 | 0.925 | 0.080 | 8 | 32543285 | intron variant | A/G | snv | 0.37 | 2 | ||
rs944289 | 0.742 | 0.200 | 14 | 36180040 | upstream gene variant | C/T | snv | 0.45 | 2 | ||
rs949963 | 0.925 | 0.160 | 2 | 102153326 | intron variant | C/T | snv | 0.22 | 2 | ||
rs9858271 | 0.925 | 0.080 | 3 | 59559604 | intron variant | G/A | snv | 0.80 | 2 | ||
rs1143633 | 0.752 | 0.280 | 2 | 112832890 | intron variant | C/G;T | snv | 1 | |||
rs11466653 | 1.000 | 0.080 | 4 | 38774614 | missense variant | A/G | snv | 6.4E-02 | 4.1E-02 | 1 |