Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2234693 | 0.555 | 0.680 | 6 | 151842200 | intron variant | T/C | snv | 0.47 | 77 | ||
rs1333049 | 0.614 | 0.520 | 9 | 22125504 | intron variant | G/C | snv | 0.41 | 60 | ||
rs2569190 | 0.620 | 0.560 | 5 | 140633331 | intron variant | A/G | snv | 0.57 | 39 | ||
rs10455872 | 0.662 | 0.320 | 6 | 160589086 | intron variant | A/G | snv | 4.3E-02 | 33 | ||
rs2383207 | 0.695 | 0.280 | 9 | 22115960 | intron variant | A/G | snv | 0.64 | 22 | ||
rs1122608 | 0.763 | 0.120 | 19 | 11052925 | intron variant | G/T | snv | 0.18 | 16 | ||
rs1271572 | 0.708 | 0.400 | 14 | 64295199 | intron variant | A/C;T | snv | 16 | |||
rs4636297 | 0.724 | 0.360 | 9 | 136670698 | intron variant | A/G | snv | 0.67 | 0.65 | 14 | |
rs146052672 | 0.851 | 0.160 | 6 | 34242693 | intron variant | -/C | delins | 5 | |||
rs974453 | 1.000 | 0.080 | 12 | 20737008 | intron variant | A/G;T | snv | 3 | |||
rs12090554 | 0.925 | 0.080 | 1 | 185583216 | intron variant | G/A | snv | 0.15 | 2 | ||
rs13290387 | 0.925 | 0.120 | 9 | 116227647 | intron variant | G/C | snv | 0.54 | 2 | ||
rs1353342 | 0.925 | 0.080 | 9 | 76259853 | intron variant | A/C | snv | 0.79 | 2 | ||
rs2227721 | 0.925 | 0.080 | 17 | 28370430 | intron variant | C/A;T | snv | 0.12 | 2 | ||
rs1140713 | 1.000 | 0.080 | 9 | 136670833 | intron variant | C/T | snv | 0.13 | 1 | ||
rs1445501474 | 1.000 | 0.080 | 18 | 22168521 | intron variant | G/T | snv | 1.4E-05 | 1 | ||
rs2824292 | 0.925 | 0.080 | 21 | 17414857 | regulatory region variant | G/A | snv | 0.47 | 3 | ||
rs72653706 | 0.695 | 0.480 | 16 | 16163078 | stop gained | G/A | snv | 1.4E-03 | 1.2E-03 | 32 | |
rs1237080661 | 0.925 | 0.080 | 3 | 38604780 | stop gained | A/G;T | snv | 2.8E-05 | 2 | ||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
rs662 | 0.485 | 0.840 | 7 | 95308134 | missense variant | T/C | snv | 0.38 | 0.42 | 157 |