Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs601338 | 0.742 | 0.280 | 19 | 48703417 | stop gained | G/A | snv | 0.38 | 0.45 | 1 | |
rs8049439 | 0.925 | 0.120 | 16 | 28826194 | intron variant | T/C;G | snv | 0.38 | 2 | ||
rs516246 | 0.925 | 0.160 | 19 | 48702915 | intron variant | C/T | snv | 0.38 | 0.45 | 2 | |
rs4833095 | 0.662 | 0.480 | 4 | 38798089 | missense variant | T/C | snv | 0.38 | 0.44 | 1 | |
rs174535 | 0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 | 8 | |
rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 5 | ||
rs1041981 | 0.667 | 0.520 | 6 | 31573007 | missense variant | C/A | snv | 0.35 | 0.38 | 2 | |
rs1142287 | 1.000 | 0.040 | 1 | 155260340 | synonymous variant | C/T | snv | 0.34 | 0.36 | 1 | |
rs7539625 | 1.000 | 0.040 | 1 | 67207082 | intron variant | G/A | snv | 0.33 | 0.30 | 1 | |
rs11230563 | 0.790 | 0.360 | 11 | 61008737 | missense variant | C/G;T | snv | 4.2E-06; 0.31 | 1 | ||
rs1050152 | 0.776 | 0.480 | 5 | 132340627 | missense variant | C/T | snv | 0.29 | 0.28 | 1 | |
rs6446272 | 1.000 | 0.040 | 3 | 49425854 | intron variant | G/A | snv | 0.28 | 0.30 | 1 | |
rs3764147 | 0.807 | 0.280 | 13 | 43883789 | missense variant | A/G | snv | 0.28 | 0.27 | 4 | |
rs2304256 | 0.732 | 0.360 | 19 | 10364976 | missense variant | C/A | snv | 0.27 | 0.23 | 3 | |
rs2108622 | 0.742 | 0.280 | 19 | 15879621 | missense variant | C/T | snv | 0.27 | 0.22 | 2 | |
rs1893592 | 0.742 | 0.280 | 21 | 42434957 | missense variant | A/C;G | snv | 0.27; 8.0E-06 | 2 | ||
rs2298428 | 0.807 | 0.240 | 22 | 21628603 | missense variant | C/T | snv | 0.27 | 0.18 | 5 | |
rs2297909 | 0.925 | 0.080 | 1 | 200991179 | intron variant | G/A | snv | 0.27 | 0.27 | 2 | |
rs16969968 | 0.653 | 0.360 | 15 | 78590583 | missense variant | G/A | snv | 0.26 | 0.24 | 1 | |
rs9858542 | 0.925 | 0.040 | 3 | 49664550 | synonymous variant | G/A | snv | 0.26 | 0.27 | 2 | |
rs3197999 | 0.732 | 0.280 | 3 | 49684099 | missense variant | G/A | snv | 0.26 | 0.27 | 6 | |
rs2024092 | 0.827 | 0.120 | 19 | 1124032 | intron variant | G/A | snv | 0.24 | 0.26 | 1 | |
rs2076753 | 1.000 | 0.040 | 16 | 50699463 | intron variant | G/A;T | snv | 0.20 | 1 | ||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 4 | |
rs2066843 | 0.925 | 0.040 | 16 | 50711288 | synonymous variant | C/A;T | snv | 0.19 | 1 |