Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 121 | |
rs1800872 | 0.495 | 0.840 | 1 | 206773062 | 5 prime UTR variant | T/G | snv | 0.69 | 119 | ||
rs1800896 | 0.507 | 0.800 | 1 | 206773552 | intron variant | T/C | snv | 0.41 | 113 | ||
rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 108 | ||
rs11209026 | 0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 | 46 | |
rs33996649 | 0.732 | 0.400 | 1 | 113852067 | missense variant | C/T | snv | 1.7E-02 | 1.6E-02 | 13 | |
rs3024490 | 0.742 | 0.520 | 1 | 206771966 | intron variant | A/C;G;T | snv | 11 | |||
rs1518111 | 0.790 | 0.360 | 1 | 206771300 | intron variant | T/C | snv | 0.71 | 9 | ||
rs3021094 | 0.827 | 0.360 | 1 | 206771607 | intron variant | T/G | snv | 8.0E-02 | 8 | ||
rs1554286 | 0.790 | 0.320 | 1 | 206770888 | 5 prime UTR variant | A/G;T | snv | 0.72 | 7 | ||
rs3790622 | 0.882 | 0.320 | 1 | 206771818 | intron variant | G/A | snv | 1.5E-03 | 3 | ||
rs7518660 | 0.925 | 0.120 | 1 | 67219760 | intron variant | G/A | snv | 0.43 | 0.47 | 2 | |
rs763059810 | 0.623 | 0.600 | 2 | 136115750 | missense variant | T/C | snv | 4.0E-06 | 41 | ||
rs17235409 | 0.653 | 0.600 | 2 | 218395009 | missense variant | G/A;C | snv | 4.9E-02; 4.1E-06 | 31 | ||
rs1372834938 | 0.763 | 0.280 | 2 | 8812465 | missense variant | G/C | snv | 4.2E-06 | 12 | ||
rs11568350 | 0.790 | 0.240 | 2 | 189565370 | missense variant | C/A | snv | 3.8E-03 | 1.6E-02 | 9 | |
rs1010 | 0.807 | 0.120 | 2 | 85581859 | 3 prime UTR variant | T/C;G | snv | 7 | |||
rs897200 | 0.851 | 0.280 | 2 | 191153045 | upstream gene variant | T/C | snv | 0.54 | 4 | ||
rs12998782 | 0.882 | 0.160 | 2 | 118967804 | intron variant | C/T | snv | 0.19 | 3 | ||
rs4252019 | 0.882 | 0.160 | 2 | 113131542 | intron variant | C/T | snv | 0.25 | 3 | ||
rs1135791 | 0.925 | 0.080 | 2 | 230177560 | missense variant | A/G | snv | 0.42 | 0.40 | 2 | |
rs12477677 | 1.000 | 0.080 | 2 | 207666398 | intron variant | T/C | snv | 0.22 | 2 | ||
rs6751745 | 0.925 | 0.080 | 2 | 118983428 | intron variant | C/T | snv | 0.31 | 2 | ||
rs9061 | 0.925 | 0.080 | 2 | 230212395 | missense variant | C/T | snv | 0.11 | 9.1E-02 | 2 | |
rs10208770 | 1.000 | 0.080 | 2 | 230170151 | intron variant | T/G | snv | 0.14 | 1 |