Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104886028 | 1.000 | 0.080 | 12 | 25227308 | missense variant | C/T | snv | 1 | |||
rs104894229 | 0.564 | 0.600 | 11 | 534289 | missense variant | C/A;G;T | snv | 23 | |||
rs1057519855 | 0.776 | 0.120 | 11 | 533873 | missense variant | CT/AC;TC | mnv | 11 | |||
rs11214077 | 0.752 | 0.120 | 11 | 112087953 | missense variant | A/G | snv | 6.6E-03 | 6.7E-03 | 12 | |
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 484 | ||
rs11554290 | 0.583 | 0.600 | 1 | 114713908 | missense variant | T/A;C;G | snv | 38 | |||
rs1188536960 | 0.882 | 0.120 | 15 | 45043305 | missense variant | A/G | snv | 5 | |||
rs121913233 | 0.627 | 0.520 | 11 | 533874 | missense variant | T/A;C;G | snv | 18 | |||
rs121913240 | 0.672 | 0.440 | 12 | 25227342 | missense variant | T/A;C;G | snv | 19 | |||
rs121913306 | 0.851 | 0.120 | 10 | 43120119 | missense variant | AGC/TTT | mnv | 4 | |||
rs121913308 | 0.827 | 0.120 | 10 | 43114492 | missense variant | A/C;G;T | snv | 4 | |||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs121913530 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 55 | |||
rs143795581 | 0.851 | 0.120 | 10 | 43114596 | missense variant | A/C;G | snv | 8.0E-06 | 2 | ||
rs145633958 | 1.000 | 0.080 | 10 | 43100551 | missense variant | C/A;T | snv | 2.7E-03; 4.0E-06 | 1 | ||
rs146646971 | 0.807 | 0.120 | 10 | 43114598 | missense variant | G/C;T | snv | 2.4E-05 | 5 | ||
rs146838520 | 0.851 | 0.120 | 10 | 43120129 | missense variant | C/T | snv | 4.0E-06 | 2.8E-05 | 4 | |
rs148935214 | 0.882 | 0.240 | 10 | 43114546 | missense variant | C/T | snv | 3.2E-04 | 3.8E-04 | 3 | |
rs1799939 | 0.658 | 0.280 | 10 | 43114671 | missense variant | G/A;C;T | snv | 0.21 | 27 | ||
rs1800863 | 0.851 | 0.160 | 10 | 43120185 | synonymous variant | C/A;G | snv | 1.6E-05; 0.21 | 4 | ||
rs183334241 | 0.925 | 0.080 | 18 | 75288186 | missense variant | G/A;C | snv | 1.6E-04 | 2 | ||
rs2075912 | 0.925 | 0.160 | 10 | 43126769 | 3 prime UTR variant | T/C | snv | 0.79 | 0.84 | 2 | |
rs2565200 | 0.925 | 0.160 | 10 | 43127485 | 3 prime UTR variant | T/A;C | snv | 2 | |||
rs3026785 | 1.000 | 0.080 | 10 | 43130238 | 3 prime UTR variant | T/C | snv | 4.3E-02 | 1 | ||
rs33927012 | 1.000 | 0.080 | 1 | 17027802 | missense variant | A/G | snv | 1.2E-02 | 9.3E-03 | 1 |