Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2965101 | 1.000 | 0.080 | 19 | 44734556 | intergenic variant | T/C | snv | 0.34 | 6 | ||
rs3024505 | 0.790 | 0.320 | 1 | 206766559 | upstream gene variant | G/A | snv | 0.11 | 6 | ||
rs3087243 | 0.623 | 0.720 | 2 | 203874196 | downstream gene variant | G/A | snv | 0.37 | 6 | ||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 24 | ||
rs3760627 | 1.000 | 0.080 | 19 | 44953923 | non coding transcript exon variant | T/C | snv | 0.80 | 0.51 | 2 | |
rs377702 | 1.000 | 0.080 | 19 | 44859410 | intron variant | G/A | snv | 0.34 | 2 | ||
rs3788013 | 0.851 | 0.240 | 21 | 42421219 | intron variant | C/A | snv | 0.44 | 1 | ||
rs3851179 | 0.752 | 0.280 | 11 | 86157598 | downstream gene variant | T/C | snv | 0.70 | 3 | ||
rs405509 | 0.667 | 0.480 | 19 | 44905579 | upstream gene variant | T/G | snv | 0.58 | 8 | ||
rs439401 | 0.851 | 0.200 | 19 | 44911194 | non coding transcript exon variant | T/C | snv | 0.68 | 4 | ||
rs4689388 | 0.882 | 0.360 | 4 | 6268329 | upstream gene variant | G/A | snv | 0.64 | 3 | ||
rs4712523 | 0.925 | 0.120 | 6 | 20657333 | intron variant | A/G | snv | 0.41 | 3 | ||
rs4788084 | 0.827 | 0.200 | 16 | 28528527 | downstream gene variant | C/T | snv | 0.36 | 3 | ||
rs5167 | 1.000 | 0.040 | 19 | 44945208 | missense variant | T/A;G | snv | 3.6E-05; 0.39 | 3 | ||
rs543293 | 0.925 | 0.080 | 11 | 86109035 | regulatory region variant | A/G | snv | 0.72 | 2 | ||
rs657152 | 0.882 | 0.200 | 9 | 133263862 | intron variant | A/C;T | snv | 14 | |||
rs6859 | 0.827 | 0.120 | 19 | 44878777 | 3 prime UTR variant | A/G | snv | 0.58 | 6 | ||
rs689 | 0.776 | 0.280 | 11 | 2160994 | splice region variant | A/T | snv | 0.73 | 0.60 | 1 | |
rs7171171 | 0.925 | 0.120 | 15 | 38614840 | intergenic variant | A/G | snv | 0.24 | 1 | ||
rs7528684 | 0.752 | 0.560 | 1 | 157701026 | upstream gene variant | A/G | snv | 0.57 | 1 | ||
rs763361 | 0.689 | 0.520 | 18 | 69864406 | missense variant | T/A;C | snv | 4.0E-06; 0.52 | 4 | ||
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 8 | |||
rs7941541 | 11 | 86147496 | intergenic variant | G/A | snv | 0.73 | 1 | ||||
rs8103315 | 1.000 | 0.080 | 19 | 44750911 | intron variant | C/A | snv | 9.1E-02 | 2 | ||
rs8106922 | 1.000 | 0.080 | 19 | 44898409 | intron variant | A/G | snv | 0.36 | 4 |