Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1048829 | 0.925 | 0.080 | 2 | 202565733 | 3 prime UTR variant | T/A;G | snv | 4 | |||
rs10491678 | 1.000 | 0.040 | 9 | 29568688 | intergenic variant | T/A;C | snv | 1 | |||
rs1050450 | 0.623 | 0.600 | 3 | 49357401 | missense variant | G/A | snv | 0.28 | 0.30 | 43 | |
rs1051052 | 1.000 | 0.040 | 14 | 94377595 | 3 prime UTR variant | A/G | snv | 0.47 | 1 | ||
rs1051730 | 0.641 | 0.600 | 15 | 78601997 | synonymous variant | G/A | snv | 0.27 | 0.26 | 43 | |
rs1051740 | 0.592 | 0.760 | 1 | 225831932 | missense variant | T/C | snv | 0.32 | 0.27 | 56 | |
rs10519203 | 0.851 | 0.080 | 15 | 78521704 | intron variant | G/A | snv | 0.67 | 8 | ||
rs10519225 | 1.000 | 0.040 | 15 | 49428581 | intron variant | G/A | snv | 0.28 | 1 | ||
rs10519717 | 0.851 | 0.080 | 4 | 144559188 | intron variant | T/C | snv | 0.21 | 4 | ||
rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
rs1059823 | 1.000 | 0.040 | 2 | 218395121 | 3 prime UTR variant | A/G | snv | 0.52 | 1 | ||
rs1061581 | 0.827 | 0.200 | 6 | 31816809 | synonymous variant | G/A | snv | 6 | |||
rs1062980 | 0.827 | 0.080 | 15 | 78500185 | 3 prime UTR variant | T/C | snv | 0.39 | 8 | ||
rs10737680 | 0.827 | 0.080 | 1 | 196710325 | intron variant | A/C | snv | 0.44 | 9 | ||
rs10759932 | 0.732 | 0.560 | 9 | 117702866 | upstream gene variant | T/C | snv | 0.18 | 15 | ||
rs10760580 | 1.000 | 0.040 | 9 | 98899368 | TF binding site variant | G/A | snv | 0.22 | 1 | ||
rs10801558 | 1.000 | 0.040 | 1 | 196729914 | intron variant | T/G | snv | 0.46 | 2 | ||
rs10801559 | 1.000 | 0.040 | 1 | 196735074 | intron variant | G/A | snv | 0.44 | 2 | ||
rs1080879 | 1.000 | 0.040 | 5 | 15054693 | intergenic variant | T/C;G | snv | 1 | |||
rs10817688 | 1.000 | 0.040 | 9 | 114943689 | intron variant | A/G | snv | 0.39 | 2 | ||
rs10851906 | 1.000 | 0.040 | 15 | 78482334 | intron variant | A/G | snv | 0.21 | 2 | ||
rs10866659 | 1.000 | 0.040 | 5 | 157510035 | intron variant | A/G;T | snv | 3 | |||
rs10873142 | 1.000 | 0.040 | 14 | 61736744 | intron variant | C/T | snv | 0.67 | 1 | ||
rs10883944 | 1.000 | 0.040 | 10 | 103891899 | intron variant | G/T | snv | 0.31 | 2 | ||
rs10890311 | 1.000 | 0.040 | 1 | 44602096 | intron variant | C/T | snv | 0.22 | 1 |