Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1400094618 | 0.882 | 0.240 | 14 | 102229508 | missense variant | A/G | snv | 3 | |||
rs1416580204 | 0.608 | 0.720 | 14 | 102250837 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 49 | |
rs782656324 | 0.925 | 0.120 | 7 | 102273394 | missense variant | C/G;T | snv | 8.1E-06 | 2 | ||
rs2548724 | 1.000 | 0.080 | 5 | 102284470 | intron variant | T/C | snv | 0.81 | 1 | ||
rs6214 | 0.672 | 0.400 | 12 | 102399791 | 3 prime UTR variant | C/T | snv | 0.45 | 26 | ||
rs6218 | 0.732 | 0.440 | 12 | 102399855 | 3 prime UTR variant | A/G | snv | 2.1E-02 | 13 | ||
rs972936 | 0.807 | 0.200 | 12 | 102431143 | intron variant | T/C | snv | 0.70 | 12 | ||
rs5742632 | 0.851 | 0.120 | 12 | 102462696 | intron variant | A/G | snv | 0.26 | 4 | ||
rs5742612 | 0.752 | 0.440 | 12 | 102481086 | intron variant | A/G | snv | 5.6E-02 | 11 | ||
rs35767 | 0.763 | 0.360 | 12 | 102481791 | upstream gene variant | A/C;G;T | snv | 13 | |||
rs363050 | 0.790 | 0.240 | 20 | 10253609 | intron variant | G/A | snv | 0.57 | 8 | ||
rs768698948 | 1.000 | 0.080 | 4 | 102579012 | missense variant | G/A;T | snv | 8.0E-06 | 1 | ||
rs7667496 | 1.000 | 0.080 | 4 | 102588298 | intron variant | C/G;T | snv | 1 | |||
rs2540317 | 1.000 | 0.080 | 2 | 102733348 | intron variant | A/G;T | snv | 1 | |||
rs4729854 | 1.000 | 0.080 | 7 | 102743216 | intron variant | T/A | snv | 0.35 | 1 | ||
rs7729395 | 1.000 | 0.080 | 5 | 102764872 | intron variant | C/T | snv | 3.1E-02 | 2 | ||
rs16869786 | 1.000 | 0.080 | 8 | 102777227 | regulatory region variant | T/C | snv | 1.4E-02 | 1 | ||
rs12147254 | 0.851 | 0.240 | 14 | 102799329 | intron variant | G/A | snv | 0.23 | 4 | ||
rs1799750 | 0.592 | 0.760 | 11 | 102799765 | intron variant | C/- | delins | 0.50 | 48 | ||
rs1004467 | 0.790 | 0.280 | 10 | 102834750 | non coding transcript exon variant | A/G | snv | 0.15 | 0.14 | 13 | |
rs17115149 | 0.882 | 0.160 | 10 | 102837961 | upstream gene variant | G/A;T | snv | 4 | |||
rs1799969 | 0.637 | 0.560 | 19 | 10284116 | missense variant | G/A | snv | 0.11 | 9.3E-02 | 38 | |
rs5498 | 0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 | 99 | |
rs12435483 | 1.000 | 0.080 | 14 | 102865271 | intron variant | C/T | snv | 0.14 | 2 | ||
rs4684677 | 0.742 | 0.360 | 3 | 10286769 | missense variant | T/A | snv | 0.10 | 6.6E-02 | 13 |