Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs1695 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 188 | |
rs16944 | 0.531 | 0.920 | 2 | 112837290 | upstream gene variant | A/G | snv | 0.57 | 92 | ||
rs28933979 | 0.587 | 0.600 | 18 | 31592974 | missense variant | G/A;C | snv | 1.0E-04 | 70 | ||
rs3834129 | 0.627 | 0.560 | 2 | 201232809 | upstream gene variant | AGTAAG/- | del | 0.48 | 38 | ||
rs76992529 | 0.653 | 0.560 | 18 | 31598655 | missense variant | G/A | snv | 1.1E-03 | 4.9E-03 | 36 | |
rs1045485 | 0.637 | 0.480 | 2 | 201284866 | missense variant | G/A;C;T | snv | 4.0E-06; 9.0E-02 | 34 | ||
rs679620 | 0.716 | 0.360 | 11 | 102842889 | missense variant | T/C | snv | 0.58 | 0.57 | 17 | |
rs1043307 | 0.776 | 0.360 | 12 | 121915890 | missense variant | A/C;G | snv | 14 | |||
rs3825172 | 0.776 | 0.360 | 12 | 121902569 | non coding transcript exon variant | C/G;T | snv | 14 | |||
rs74421874 | 0.776 | 0.360 | 12 | 121902546 | non coding transcript exon variant | G/A | snv | 0.24 | 14 | ||
rs1800012 | 0.763 | 0.320 | 17 | 50200388 | intron variant | C/A | snv | 0.14 | 13 | ||
rs3791679 | 0.925 | 0.120 | 2 | 55869757 | intron variant | A/G | snv | 0.20 | 11 | ||
rs12722 | 0.882 | 0.120 | 9 | 134842570 | 3 prime UTR variant | C/T | snv | 0.44 | 6 | ||
rs370579379 | 0.827 | 0.160 | 10 | 93594018 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 6 | |
rs121918082 | 0.827 | 0.280 | 18 | 31595244 | missense variant | G/C | snv | 6 | |||
rs958191819 | 0.851 | 0.240 | 18 | 31595212 | missense variant | A/T | snv | 7.0E-06 | 6 | ||
rs72755233 | 1.000 | 0.080 | 15 | 100152748 | missense variant | G/A;T | snv | 7.1E-02; 3.2E-05 | 5 | ||
rs62621197 | 1.000 | 0.080 | 19 | 8605262 | missense variant | C/A;T | snv | 4.1E-06; 3.1E-02 | 2.9E-02 | 4 | |
rs121918088 | 0.851 | 0.120 | 18 | 31598631 | missense variant | T/C | snv | 4 | |||
rs486055 | 0.925 | 0.120 | 11 | 102779693 | missense variant | C/G;T | snv | 1.2E-05; 0.10 | 3 | ||
rs267607247 | 0.882 | 0.120 | 1 | 161305953 | missense variant | C/A | snv | 3 | |||
rs121918091 | 0.882 | 0.200 | 18 | 31595169 | missense variant | T/C | snv | 4.0E-06 | 3 | ||
rs1863190 | 1.000 | 0.080 | 2 | 217263429 | non coding transcript exon variant | A/T | snv | 0.53 | 2 | ||
rs13113 | 0.925 | 0.200 | 2 | 201287439 | 3 prime UTR variant | T/A | snv | 0.33 | 2 |