Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17780256 | 0.827 | 0.120 | 17 | 72646784 | 3 prime UTR variant | A/C | snv | 0.18 | 6 | ||
rs1517352 | 0.851 | 0.160 | 2 | 191066738 | intron variant | A/C | snv | 0.45 | 3 | ||
rs2382817 | 0.925 | 0.040 | 2 | 218286495 | 5 prime UTR variant | A/C | snv | 0.61 | 3 | ||
rs6017342 | 0.925 | 0.120 | 20 | 44436388 | non coding transcript exon variant | A/C | snv | 0.62 | 2 | ||
rs7165170 | 1.000 | 0.040 | 15 | 90638257 | non coding transcript exon variant | A/C | snv | 0.26 | 2 | ||
rs2395022 | 7 | 99152756 | intergenic variant | A/C | snv | 0.93 | 1 | ||||
rs12720356 | 0.752 | 0.360 | 19 | 10359299 | missense variant | A/C;G | snv | 6.1E-02; 4.0E-06 | 7 | ||
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 7 | ||
rs798502 | 1.000 | 0.040 | 7 | 2750246 | intron variant | A/C;G | snv | 4 | |||
rs10051722 | 1.000 | 0.040 | 5 | 130768383 | intron variant | A/C;G | snv | 2 | |||
rs10142466 | 14 | 68805067 | intergenic variant | A/C;G;T | snv | 1 | |||||
rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 7 | ||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 34 | |
rs1535 | 0.752 | 0.240 | 11 | 61830500 | intron variant | A/G | snv | 0.31 | 18 | ||
rs2111485 | 0.724 | 0.280 | 2 | 162254026 | regulatory region variant | A/G | snv | 0.46 | 12 | ||
rs1893217 | 0.742 | 0.440 | 18 | 12809341 | intron variant | A/G | snv | 0.12 | 10 | ||
rs17622378 | 0.790 | 0.200 | 5 | 132442760 | intron variant | A/G | snv | 0.28 | 8 | ||
rs6740847 | 0.925 | 0.040 | 2 | 181443625 | intergenic variant | A/G | snv | 0.57 | 8 | ||
rs34920465 | 0.807 | 0.160 | 1 | 22373858 | intergenic variant | A/G | snv | 0.24 | 7 | ||
rs13407913 | 0.827 | 0.120 | 2 | 24874775 | intron variant | A/G | snv | 0.54 | 6 | ||
rs2284553 | 0.776 | 0.240 | 21 | 33404389 | intron variant | A/G | snv | 0.69 | 6 | ||
rs2538470 | 0.827 | 0.120 | 7 | 148523356 | intergenic variant | A/G | snv | 0.61 | 6 | ||
rs2816958 | 0.827 | 0.120 | 1 | 200132792 | intron variant | A/G | snv | 0.84 | 6 | ||
rs7608910 | 0.827 | 0.120 | 2 | 60977721 | intron variant | A/G | snv | 0.37 | 6 | ||
rs10761659 | 0.925 | 0.040 | 10 | 62685804 | intron variant | A/G | snv | 0.43 | 3 |