Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 24 | ||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 13 | |
rs11065987 | 0.807 | 0.280 | 12 | 111634620 | intergenic variant | A/G | snv | 0.29 | 12 | ||
rs7574865 | 0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 | 8 | ||
rs2872507 | 0.752 | 0.360 | 17 | 39884510 | intergenic variant | G/A;T | snv | 7 | |||
rs2305480 | 0.763 | 0.280 | 17 | 39905943 | missense variant | G/A | snv | 0.40 | 0.35 | 7 | |
rs10488631 | 0.742 | 0.280 | 7 | 128954129 | upstream gene variant | T/C | snv | 9.0E-02 | 7 | ||
rs8067378 | 0.752 | 0.240 | 17 | 39895095 | regulatory region variant | A/G | snv | 0.50 | 6 | ||
rs3087243 | 0.623 | 0.720 | 2 | 203874196 | downstream gene variant | G/A | snv | 0.37 | 6 | ||
rs2290400 | 0.790 | 0.360 | 17 | 39909987 | intron variant | T/C | snv | 0.48 | 6 | ||
rs7774434 | 0.807 | 0.360 | 6 | 32689801 | TF binding site variant | T/C | snv | 0.40 | 5 | ||
rs393152 | 0.851 | 0.160 | 17 | 45641777 | non coding transcript exon variant | A/G | snv | 0.18 | 0.29 | 5 | |
rs1864325 | 0.882 | 0.160 | 17 | 45900461 | intron variant | C/T | snv | 0.14 | 5 | ||
rs8070723 | 0.851 | 0.240 | 17 | 46003698 | intron variant | A/G | snv | 0.18 | 5 | ||
rs738409 | 0.557 | 0.720 | 22 | 43928847 | missense variant | C/G | snv | 0.28 | 0.22 | 5 | |
rs2856683 | 0.827 | 0.320 | 6 | 32687441 | regulatory region variant | T/A;C;G | snv | 0.25 | 4 | ||
rs3135363 | 0.776 | 0.360 | 6 | 32421871 | intergenic variant | A/G | snv | 0.24 | 4 | ||
rs9357152 | 0.827 | 0.240 | 6 | 32697183 | regulatory region variant | A/G | snv | 0.24 | 4 | ||
rs12708716 | 0.807 | 0.320 | 16 | 11086016 | intron variant | A/G | snv | 0.37 | 4 | ||
rs2305479 | 0.882 | 0.160 | 17 | 39905964 | missense variant | C/T | snv | 0.43 | 0.39 | 4 | |
rs7219923 | 0.882 | 0.160 | 17 | 39918265 | non coding transcript exon variant | C/T | snv | 0.52 | 4 | ||
rs9303281 | 0.882 | 0.160 | 17 | 39917793 | non coding transcript exon variant | G/A | snv | 0.50 | 4 | ||
rs9303277 | 0.790 | 0.240 | 17 | 39820216 | intron variant | C/T | snv | 0.52 | 4 | ||
rs694739 | 0.763 | 0.320 | 11 | 64329761 | upstream gene variant | A/G | snv | 0.28 | 4 | ||
rs17651549 | 0.882 | 0.160 | 17 | 45983912 | missense variant | C/T | snv | 0.15 | 0.14 | 4 |