Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs77294580 | 1.000 | 0.040 | 17 | 63480396 | missense variant | G/A;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
rs782591769 | 1.000 | 0.040 | 7 | 74045237 | missense variant | G/C | snv | 8.0E-06 | 1 | ||
rs8125581 | 1.000 | 0.040 | 20 | 46010604 | missense variant | G/A | snv | 3.0E-04 | 3.4E-04 | 1 | |
rs9316871 | 1.000 | 0.040 | 13 | 22287782 | intergenic variant | A/G | snv | 0.22 | 1 | ||
rs602633 | 0.851 | 0.080 | 1 | 109278889 | downstream gene variant | T/G | snv | 0.63 | 10 | ||
rs595244 | 0.882 | 0.080 | 15 | 48548638 | intron variant | C/T | snv | 7.7E-02 | 3 | ||
rs764522 | 0.882 | 0.080 | 3 | 30605058 | upstream gene variant | G/A;C | snv | 3 | |||
rs7866503 | 0.882 | 0.080 | 9 | 22091925 | intron variant | G/T | snv | 0.50 | 3 | ||
rs8087799 | 0.882 | 0.080 | 18 | 22605468 | regulatory region variant | G/A | snv | 0.43 | 3 | ||
rs919433 | 0.882 | 0.080 | 2 | 197301841 | intron variant | G/A | snv | 0.38 | 3 | ||
rs201191171 | 0.925 | 0.080 | 20 | 46013279 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06 | 2 | ||
rs326118 | 0.925 | 0.080 | 5 | 7868430 | intron variant | T/G | snv | 0.21 | 2 | ||
rs773474756 | 0.925 | 0.080 | 11 | 102790467 | missense variant | T/C | snv | 8.1E-06 | 2 | ||
rs6511720 | 0.790 | 0.120 | 19 | 11091630 | intron variant | G/T | snv | 0.12 | 15 | ||
rs5516 | 0.827 | 0.120 | 19 | 50820217 | missense variant | C/G | snv | 0.69 | 0.67 | 6 | |
rs1057335 | 0.827 | 0.120 | 17 | 1754359 | missense variant | G/A | snv | 0.22 | 0.20 | 5 | |
rs12191786 | 0.851 | 0.120 | 6 | 22004398 | intron variant | C/A;T | snv | 4 | |||
rs486055 | 0.925 | 0.120 | 11 | 102779693 | missense variant | C/G;T | snv | 1.2E-05; 0.10 | 3 | ||
rs3019885 | 0.925 | 0.120 | 8 | 117013406 | intron variant | T/A;G | snv | 2 | |||
rs4988300 | 0.925 | 0.120 | 11 | 68321363 | intron variant | G/T | snv | 0.50 | 2 | ||
rs1466535 | 0.790 | 0.160 | 12 | 57140687 | intron variant | G/A;C | snv | 9 | |||
rs3877899 | 0.827 | 0.160 | 5 | 42801166 | missense variant | C/A;T | snv | 4.0E-06; 0.20 | 7 | ||
rs12692386 | 0.827 | 0.160 | 2 | 9555777 | 5 prime UTR variant | A/G | snv | 0.72 | 5 | ||
rs1524668 | 0.851 | 0.160 | 2 | 9557243 | upstream gene variant | A/C | snv | 0.64 | 4 | ||
rs8003379 | 0.882 | 0.160 | 14 | 64406881 | intron variant | A/C | snv | 0.23 | 3 |