Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2042329 | 0.882 | 0.120 | 5 | 64771925 | intron variant | T/C;G | snv | 3 | |||
rs2074647 | 0.882 | 0.120 | 14 | 72562470 | missense variant | G/A | snv | 9.0E-02 | 0.10 | 3 | |
rs2228104 | 0.882 | 0.120 | 7 | 75985635 | synonymous variant | T/A;C | snv | 4.5E-06; 0.92 | 3 | ||
rs2664139 | 0.882 | 0.120 | 15 | 39580382 | upstream gene variant | T/C | snv | 0.41 | 3 | ||
rs3213255 | 0.882 | 0.120 | 19 | 43573355 | intron variant | G/A | snv | 0.60 | 3 | ||
rs3213356 | 0.882 | 0.120 | 19 | 43554087 | intron variant | C/T | snv | 0.60 | 3 | ||
rs3219493 | 0.882 | 0.120 | 1 | 45330597 | intron variant | G/C | snv | 0.92 | 0.93 | 3 | |
rs377062126 | 0.882 | 0.120 | 12 | 104319543 | missense variant | G/A | snv | 2.1E-05 | 3.5E-05 | 3 | |
rs4969054 | 0.882 | 0.120 | 17 | 73016334 | intron variant | G/C | snv | 0.73 | 3 | ||
rs4986826 | 0.882 | 0.120 | 7 | 17339533 | missense variant | G/A | snv | 7.8E-03 | 2.2E-02 | 3 | |
rs62185668 | 0.925 | 0.120 | 20 | 10981287 | intron variant | C/A | snv | 0.19 | 3 | ||
rs6464268 | 0.882 | 0.120 | 7 | 152684065 | intergenic variant | A/G | snv | 0.23 | 3 | ||
rs715021 | 0.882 | 0.120 | 2 | 221196620 | intergenic variant | C/G | snv | 0.26 | 3 | ||
rs72552316 | 0.882 | 0.120 | X | 12889591 | 3 prime UTR variant | T/C | snv | 3 | |||
rs7257330 | 0.882 | 0.120 | 19 | 29810916 | upstream gene variant | G/A | snv | 0.30 | 3 | ||
rs7431 | 0.882 | 0.120 | 8 | 22540949 | 3 prime UTR variant | G/A | snv | 0.56 | 3 | ||
rs758057623 | 0.882 | 0.120 | 11 | 67584520 | missense variant | G/A | snv | 3 | |||
rs771866347 | 0.882 | 0.120 | 3 | 49358109 | missense variant | G/A | snv | 4.1E-06 | 3 | ||
rs7832529 | 0.882 | 0.120 | 8 | 42449295 | intron variant | T/C | snv | 0.24 | 3 | ||
rs8041357 | 0.882 | 0.120 | 15 | 74577097 | intron variant | T/C | snv | 6.6E-02 | 3 | ||
rs8102137 | 0.882 | 0.120 | 19 | 29805946 | regulatory region variant | T/C | snv | 0.24 | 3 | ||
rs8444 | 0.882 | 0.120 | 1 | 150966095 | 3 prime UTR variant | G/A | snv | 0.35 | 3 | ||
rs861531 | 0.882 | 0.120 | 14 | 103706470 | 3 prime UTR variant | C/A | snv | 0.32 | 3 | ||
rs921142 | 0.882 | 0.120 | 8 | 41311757 | upstream gene variant | T/C | snv | 0.31 | 3 | ||
rs9624880 | 0.882 | 0.120 | 22 | 25588025 | intron variant | C/T | snv | 3 |