Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10011025 | 1.000 | 0.120 | 4 | 174733072 | intron variant | A/C;G | snv | 1 | |||
rs1001179 | 0.641 | 0.680 | 11 | 34438684 | upstream gene variant | C/T | snv | 0.16 | 33 | ||
rs1003878 | 0.882 | 0.200 | 6 | 32332045 | stop gained | G/A | snv | 0.19 | 0.23 | 3 | |
rs1004446 | 0.827 | 0.240 | 11 | 2148913 | intron variant | G/A | snv | 0.37 | 7 | ||
rs1012411 | 1.000 | 0.120 | 6 | 30364778 | upstream gene variant | T/G | snv | 0.32 | 1 | ||
rs1015166 | 0.925 | 0.120 | 6 | 32830954 | intron variant | C/G;T | snv | 0.28 | 2 | ||
rs10181656 | 0.763 | 0.360 | 2 | 191105153 | intron variant | G/C | snv | 0.79 | 9 | ||
rs10186193 | 1.000 | 0.120 | 2 | 3550384 | synonymous variant | T/C | snv | 0.33 | 0.41 | 1 | |
rs1020856343 | 0.851 | 0.240 | 5 | 132393705 | missense variant | C/T | snv | 4.0E-06 | 5 | ||
rs1022059218 | 0.925 | 0.200 | 2 | 203936863 | missense variant | G/A | snv | 2 | |||
rs1023934247 | 1.000 | 0.120 | 10 | 70598292 | missense variant | G/C;T | snv | 1 | |||
rs10255021 | 1.000 | 0.120 | 7 | 94402493 | intron variant | G/A | snv | 0.13 | 1 | ||
rs10272724 | 0.882 | 0.200 | 7 | 50409515 | downstream gene variant | T/C | snv | 0.24 | 4 | ||
rs10277986 | 1.000 | 0.120 | 7 | 50961290 | intron variant | T/A;C | snv | 1 | |||
rs10336 | 0.851 | 0.240 | 4 | 76001835 | 3 prime UTR variant | A/G;T | snv | 4 | |||
rs1041740 | 0.807 | 0.320 | 21 | 31667849 | intron variant | C/T | snv | 0.24 | 8 | ||
rs1041981 | 0.667 | 0.520 | 6 | 31573007 | missense variant | C/A | snv | 0.35 | 0.38 | 25 | |
rs1042713 | 0.576 | 0.800 | 5 | 148826877 | missense variant | G/A | snv | 0.42 | 0.43 | 63 | |
rs10484566 | 0.925 | 0.200 | 6 | 32867481 | regulatory region variant | T/G | snv | 6.8E-02 | 2 | ||
rs1048990 | 0.790 | 0.280 | 14 | 35292469 | 5 prime UTR variant | C/G;T | snv | 0.19; 4.0E-06 | 8 | ||
rs10492166 | 1.000 | 0.120 | 12 | 9733403 | upstream gene variant | G/A | snv | 0.50 | 1 | ||
rs1050152 | 0.776 | 0.480 | 5 | 132340627 | missense variant | C/T | snv | 0.29 | 0.28 | 10 | |
rs10509540 | 0.925 | 0.160 | 10 | 88263276 | upstream gene variant | T/C | snv | 0.25 | 2 | ||
rs10517086 | 0.882 | 0.160 | 4 | 26083889 | intron variant | G/A | snv | 0.27 | 4 | ||
rs1052486 | 0.851 | 0.200 | 6 | 31642909 | missense variant | A/G | snv | 0.51 | 0.44 | 4 |