Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
rs854560 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 113 | ||
rs1188383936 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 102 | ||
rs899127658 | 0.547 | 0.720 | 11 | 46739084 | missense variant | G/A;C | snv | 82 | |||
rs751377893 | 0.574 | 0.680 | 1 | 169546513 | missense variant | T/C | snv | 4.0E-06 | 65 | ||
rs4673 | 0.653 | 0.600 | 16 | 88646828 | missense variant | A/G;T | snv | 0.70 | 32 | ||
rs1387153 | 0.807 | 0.200 | 11 | 92940662 | downstream gene variant | C/G;T | snv | 10 | |||
rs3761959 | 0.827 | 0.320 | 1 | 157699488 | intron variant | C/A;G;T | snv | 7 | |||
rs28357984 | 0.851 | 0.160 | MT | 5178 | missense variant | C/A | snv | 6 | |||
rs779829591 | 0.827 | 0.320 | 1 | 94532395 | missense variant | G/A | snv | 4.0E-06 | 5 | ||
rs3840634 | 0.925 | 0.120 | 7 | 116556798 | intron variant | T/C | snv | 2 | |||
rs10489678 | 1.000 | 0.120 | 1 | 157699878 | intron variant | G/A;C;T | snv | 1 | |||
rs10955255 | 1.000 | 0.120 | 8 | 101524177 | intron variant | A/G;T | snv | 1 | |||
rs1264525329 | 1.000 | 0.120 | 6 | 159682587 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
rs611419 | 1.000 | 0.120 | 8 | 101491489 | intron variant | T/A;C | snv | 1 | |||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs3805435 | 0.882 | 0.120 | 5 | 151021735 | non coding transcript exon variant | T/C | snv | 8.4E-02 | 3 | ||
rs3736309 | 0.925 | 0.120 | 12 | 49964271 | intron variant | A/G | snv | 0.12 | 2 | ||
rs5370 | 0.630 | 0.520 | 6 | 12296022 | missense variant | G/T | snv | 0.23 | 0.21 | 37 | |
rs1805087 | 0.496 | 0.800 | 1 | 236885200 | missense variant | A/G | snv | 0.20 | 0.21 | 135 | |
rs6989650 | 1.000 | 0.120 | 8 | 101669109 | 3 prime UTR variant | C/T | snv | 0.24 | 1 | ||
rs2075800 | 0.776 | 0.440 | 6 | 31810169 | missense variant | C/T | snv | 0.32 | 0.25 | 8 | |
rs755622 | 0.611 | 0.720 | 22 | 23894205 | intron variant | G/C | snv | 0.26 | 44 | ||
rs7493 | 0.677 | 0.440 | 7 | 95405463 | missense variant | G/C | snv | 0.27 | 0.27 | 24 | |
rs1050450 | 0.623 | 0.600 | 3 | 49357401 | missense variant | G/A | snv | 0.28 | 0.30 | 43 |