Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10503669 | 0.925 | 0.080 | 8 | 19990179 | intergenic variant | C/A | snv | 8.4E-02 | 7 | ||
rs173539 | 0.882 | 0.080 | 16 | 56954132 | intergenic variant | C/T | snv | 0.33 | 7 | ||
rs1883025 | 0.807 | 0.120 | 9 | 104902020 | intron variant | C/T | snv | 0.28 | 7 | ||
rs2266788 | 0.763 | 0.440 | 11 | 116789970 | 3 prime UTR variant | G/A | snv | 0.93 | 7 | ||
rs3782886 | 0.724 | 0.480 | 12 | 111672685 | synonymous variant | T/C | snv | 1.9E-02 | 5.9E-03 | 7 | |
rs2383207 | 0.695 | 0.280 | 9 | 22115960 | intron variant | A/G | snv | 0.64 | 7 | ||
rs1800775 | 0.790 | 0.240 | 16 | 56961324 | upstream gene variant | C/A;G | snv | 0.51; 5.7E-06 | 7 | ||
rs1421085 | 0.752 | 0.280 | 16 | 53767042 | intron variant | T/C | snv | 0.31 | 7 | ||
rs328 | 0.732 | 0.440 | 8 | 19962213 | stop gained | C/G | snv | 9.2E-02 | 9.0E-02 | 7 | |
rs560887 | 0.827 | 0.120 | 2 | 168906638 | intron variant | T/C | snv | 0.79 | 0.80 | 7 | |
rs2075290 | 0.882 | 0.160 | 11 | 116782580 | intron variant | C/G;T | snv | 7 | |||
rs6589566 | 0.882 | 0.080 | 11 | 116781707 | intron variant | G/A;C;T | snv | 7 | |||
rs17410962 | 1.000 | 0.040 | 8 | 19990569 | intergenic variant | G/A | snv | 0.15 | 6 | ||
rs17782313 | 0.683 | 0.480 | 18 | 60183864 | intergenic variant | T/C | snv | 0.24 | 6 | ||
rs2083637 | 0.925 | 0.080 | 8 | 20007664 | intergenic variant | A/G | snv | 0.25 | 6 | ||
rs7138803 | 0.827 | 0.240 | 12 | 49853685 | intergenic variant | G/A;T | snv | 6 | |||
rs651821 | 0.851 | 0.360 | 11 | 116791863 | 5 prime UTR variant | C/T | snv | 0.88 | 0.89 | 6 | |
rs662799 | 0.689 | 0.480 | 11 | 116792991 | upstream gene variant | G/A | snv | 0.90 | 6 | ||
rs1919128 | 0.882 | 0.120 | 2 | 27578892 | missense variant | A/G | snv | 0.30 | 0.24 | 6 | |
rs1333049 | 0.614 | 0.520 | 9 | 22125504 | intron variant | G/C | snv | 0.41 | 6 | ||
rs711752 | 1.000 | 0.040 | 16 | 56962299 | splice region variant | G/A;C | snv | 6 | |||
rs9939224 | 1.000 | 0.040 | 16 | 56968820 | intron variant | T/G | snv | 0.75 | 6 | ||
rs9940128 | 0.851 | 0.120 | 16 | 53766842 | intron variant | G/A | snv | 0.42 | 6 | ||
rs3749147 | 0.882 | 0.120 | 2 | 27629051 | missense variant | G/A | snv | 0.23 | 0.20 | 6 | |
rs13022873 | 0.882 | 0.120 | 2 | 27592643 | intron variant | A/C;T | snv | 6 |