Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1049194905 | 0.925 | 0.080 | 3 | 38604063 | synonymous variant | A/G | snv | 2 | |||
rs1237080661 | 0.925 | 0.080 | 3 | 38604780 | stop gained | A/G;T | snv | 2.8E-05 | 2 | ||
rs184934308 | 0.925 | 0.080 | 3 | 38575342 | synonymous variant | G/A | snv | 4.1E-04 | 9.1E-05 | 2 | |
rs750678689 | 0.925 | 0.080 | 3 | 38566466 | synonymous variant | G/A | snv | 8.0E-06 | 2.1E-05 | 2 | |
rs6125 | 0.925 | 0.080 | 1 | 169613079 | missense variant | C/T | snv | 5.6E-02 | 5.2E-02 | 2 | |
rs2227721 | 0.925 | 0.080 | 17 | 28370430 | intron variant | C/A;T | snv | 0.12 | 2 | ||
rs2824292 | 0.925 | 0.080 | 21 | 17414857 | regulatory region variant | G/A | snv | 0.47 | 3 | ||
rs61688134 | 0.882 | 0.080 | 12 | 21864476 | missense variant | C/T | snv | 7.4E-03 | 7.5E-03 | 3 | |
rs1805120 | 0.882 | 0.080 | 7 | 150952443 | synonymous variant | G/A | snv | 0.30 | 0.26 | 3 | |
rs1050286 | 0.882 | 0.160 | 12 | 10158964 | 3 prime UTR variant | T/C | snv | 0.40 | 3 | ||
rs3745601 | 0.882 | 0.120 | 19 | 10113872 | missense variant | G/A | snv | 0.16 | 0.13 | 3 | |
rs200034939 | 0.882 | 0.080 | 3 | 38557248 | missense variant | C/A | snv | 3.2E-05 | 3 | ||
rs974453 | 1.000 | 0.080 | 12 | 20737008 | intron variant | A/G;T | snv | 3 | |||
rs1233347077 | 0.851 | 0.160 | 19 | 44905894 | missense variant | G/C | snv | 7.0E-06 | 4 | ||
rs1187513719 | 0.851 | 0.200 | 10 | 94780595 | missense variant | A/G | snv | 4.0E-06 | 4 | ||
rs41508050 | 0.882 | 0.080 | 14 | 61738090 | missense variant | C/T | snv | 3.8E-03 | 4.0E-03 | 4 | |
rs199473244 | 0.851 | 0.120 | 3 | 38557251 | missense variant | C/A | snv | 4 | |||
rs762890235 | 0.827 | 0.240 | X | 15578220 | missense variant | G/T | snv | 3.8E-05 | 9.5E-06 | 5 | |
rs1799943 | 0.925 | 0.080 | 13 | 32316435 | 5 prime UTR variant | G/A;C;T | snv | 0.25 | 5 | ||
rs225015 | 0.882 | 0.160 | 14 | 80201236 | 3 prime UTR variant | G/A | snv | 0.37 | 5 | ||
rs146052672 | 0.851 | 0.160 | 6 | 34242693 | intron variant | -/C | delins | 5 | |||
rs770572030 | 0.827 | 0.160 | 18 | 49581427 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 5 | ||
rs1805017 | 0.851 | 0.240 | 6 | 46716485 | missense variant | C/A;T | snv | 4.0E-06; 0.31 | 5 | ||
rs11571836 | 0.827 | 0.200 | 13 | 32399302 | 3 prime UTR variant | A/G;T | snv | 6 | |||
rs1064039 | 0.827 | 0.200 | 20 | 23637790 | missense variant | C/G;T | snv | 0.20 | 6 |